CAS: 527-85-5; 2-Methylbenzamide

该化合物是属于苯胺衍生物类别的有机化合物,在苯环的正方位上有一个甲基替代物,影响其反应性和物理特性,该化合物通常用作制药和农用化学合成的中间体,因其多用途氨化物功能和稳定的芳香核心,其晶状固体形式和有机溶剂中的中溶性适合受控反应. 2-甲基乙基苯并氨因其在生产专门精细化学品方面的作用而备受重视,在需要进行精确的结构修改的情况下,建议适当处理和储存以保持其稳定性和纯性.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

N-羟基-2-甲基苯甲酰胺 2-Methylphenylhydroxamic Acid 17512-73-1
2-甲苯甲酰肼 2-Methylbenzohydrazide 7658-80-2
2-甲基异硫氰酸苯甲酰酯 2-Methylbenzoyl Isothiocyanate 28115-85-7
苯甲酰胺 Benzamide 55-21-0
Di-O-Toluoyl-Amine
2-(三氟甲基)苯甲酰胺 2-(Trifluoromethyl)Benzamide 360-64-5
2-甲基苯甲基胺 Ortho-Methylbenzylamine 89-93-0
2-甲基苯甲醛 2-Methylphenyl Aldehyde 529-20-4

合成工艺路线路线简述

  • 合成目标产物 O-Toluamide 主要起始原料 2-Methylbenzaldehyde
  • (文献来源)合成步骤主要原料 2-Methylbenzaldehyde
📜3-乙基甲苯置于叔丁基过氧化氢,氨,碘体系中,用 水 作为反应溶剂,化学反应 3.0H,以73%的收率获得产物2-甲基苯甲酰胺
参考文献:Iodine-Mediated Domino Protocol For The Synthesis Of Benzamides From Ethylarenes Via Sp3 C-h Functionalization
标题:Iodine-Mediated Domino Protocol For The Synthesis Of Benzamides From Ethylarenes Via Sp3 C-h Functionalization
摘要:An Efficient,Metal-Free Domino Protocol For The Synthesis Of Benzamides Has Been Developed From Ethylarenes Using Aqueous Ammonia. The Reaction Proceeds Through The Formation Of Triiodomethyl Ketone Intermediate In The Presence Of Iodine As The Promoter And Tbhp As An Oxidant Followed By Nucleophilic Substitution With Aqueous Ammonia,Forming An Amide. This Operationally Simple,Functional-Group-Tolerant Tandem Approach Provides An Easy Access To The Broad Range Of Biologically Important Benzamides.
DOI:10.1055/s-0034-1380210

海关参考信息

专利信息


专利号:US-10611864-B2
优先权日:2015-09-22
标 题:Synthesis of substituted amidobenzoate compounds, the compounds obtained and the use thereof as phthalate free internal electron donor for polymerization of olefins
发明人:ZUIDEVELD MARTIN ALEXANDER; SAINANI JAIPRAKASH BRIJLAL; AL-HUMAIDAN OSAMAH; PADMANABHAN SUDHAKAR R; SHINGE PRASHANT SUKUMAR; SHETTY SHARANKUMAR G; SHAIKH ABBAS-ALLI GHUDUBHAI
权利人:SABIC GLOBAL TECHNOLOGIES BV
摘要:The present invention relates to a compound according to Formula (I) wherein R 1 is a hydrocarbyl group selected from the group consisting of alkyl, alkenyl, aryl, aralkyl, and alkylaryl groups, and one or more combinations thereof; wherein R 2 is a hydrogen atom, an aryl group or an alkyl group; and wherein R 3 , R 4 , R 5 and R 6 , are the same or different and are each independently a hydrogen atom, a halogen atom, a cyano group, an amino group, a hydrocarbyl group selected from the group consisting of alkyl, alkenyl, aryl, aralkyl, and alkylaryl groups or an alkoxy group, and one or more combinations thereof as internal electron donor and to a process for the synthesis of a compound according to Formula (I), wherein R 1 is a hydrocarbyl group selected from the group consisting of alkyl, alkenyl, aryl, aralkyl, alkoxycarbonyl and alkylaryl groups, and one or more combinations thereof; wherein R 2 is a hydrogen atom or an alkyl group; wherein R 3 , R 4 , R 5 and R 6 , are the same or different and are each independently selected from a group consisting of a hydrogen atom; a hydrocarbyl, preferably, said process comprising the step of reacting a compound according to Formula (II) [R 1 —C(â•?O)Cl] with a compound according to Formula (III) to obtain the compound according to Formula (I) and to the use of these compounds as internal donor in Ziegler-Natta catalysis of lefins.

专利号:US-5097065-A
优先权日:1985-04-05
标题:Process for synthesis of a novel amino acid from styrene, acetamide and syngas
发明人:LIN JIANG-JEN
权利人:TEXACO INC
摘要:A phenyl substituted amino acid derivative is synthesized by reacting styrene, acetamide and synthesis gas with a bimetallic catalyst comprising a rhodium-containing compound and a cobalt-containing compound, optionally in the presence of a solvent at a pressure of at least 500 psi and a temperature of at least 50° C. The novel amino acid contains a carboxylic acid group, an acetamido group at the alpha-position and a phenyl group at the beta-position.

专利号:US-4042600-A
优先权日:1972-10-17
标 题 :Pyrolysis of 2-sulfochloride benzoates
发明人:DIPIPPO CARMINE A
权利人:SCOTT PAPER CO
摘要:Ortho-sulfobenzoic anhydride is synthesized by pyrolysis of the 2-sulfochloride benzoates. The benzoate intermediates are readily prepared by reacting either the esters of dithiodibenzoic acid with chloride water or the 2-diazonium chloride benzoates with sulfur dioxide. The invention also provides for the total synthesis of saccharin, free of bitter tasting contaminants, from such reactants, the ultimate step in such synthesis being the ammonolysis of the o-sulfobenzoic anhydride.

专利号:US-4892687-A
优先权日:1986-10-08
标题:Process for synthesis of amidoacids using a cobalt catalyst and a bidental phosphine ligand
发明人:LIN JIANG-JEN
权利人:TEXACO INC
摘要:A process is disclosed for producing N-acetyl-aminoacid which comprises reacting a feedstock from the group consisting of simple olefins, acetamide and synthesis gas with a catalyst comprising a cobalt-containing compound promoted by a bidental-phosphine ligand in a solvent at a pressure of 500 psi or greater and a temperature of 50 DEG C. or greater. The presence of the ligand increases both reaction rate and cobalt catalyst stability.

专利号:US-4891442-A
优先权日:1987-03-09
标 题 :Process for synthesis of β-phenylalanine
发明人:LIN JIANG-JEN; KNIFTON JOHN F
权利人:TEXACO INC
摘要:N-acetyl-β-phenylalanine is synthesized by reacting phenylacetaldehyde, acetamide and synthesis gas with a catalyst comprising a cobalt-containing compound in conjunction with a cocatalyst that may be either a Group VB or VIB containing ligand, or a rhodium compound optionally bonded to one or more Group VB or VIB donor ligands, at a temperature of at least 50° C. and a pressure of at least 500 psi.

专利号:US-10266467-B2
优先权日:2017-08-02
标 题:Synthesis of glycols via transfer hydrogenation of alpha-functional esters with alcohols
发明人:CHAKRABORTY SUMIT; HEMBRE ROBERT THOMAS
权利人:EASTMAN CHEM CO
摘要:A transfer hydrogenation process for forming vicinal diols by hydrogenating 1,2-dioxygenated organic compounds using alcohols as the reducing agent instead of the traditional H 2 gas. The transfer hydrogenation is carried out under milder conditions of temperature and pressure than is typical for ester hydrogenation with H 2 . The milder conditions of operation provide benefits, such as lower operating and capital costs for industrial scale production as well as savings in product purification due to the avoidance of by-products from exposure of reaction mixtures and products to high temperatures.

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品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献

[参考文献]: Thanh Nguyen Le, Et Al. First Total Synthesis Of The Phenolic 7,8-Dihydro-8-Oxoprotoberberine Alkaloid, Cerasonine. Chem Pharm Bull (Tokyo). 2008 Jul;56(7):1026-9.

合成参考文献


摘要:Khartulyari, A.; Maier, M. E., Science of Synthesis Knowledge Updates, (2010) 3, 80.
摘要:Zhdankin, V. V., Science of Synthesis Knowledge Updates, (2015) 1, 283.
摘要:Asano, Y., Science of Synthesis: Biocatalysis in Organic Synthesis, (2015) 1, 258.
摘要:Biffis, A.; Tubaro, C., Science of Synthesis: N-Heterocyclic Carbenes in Catalytic Organic Synthesis, (2016) 1, 420.
参考文献:10.1007/bf02975091
摘要:Cheon SH, Park JS, Lee JY, Lee YN, Yi H, Chung BH, Choi BG, Cho WJ, Choi SU, Lee CO. Structure-activity relationship studies of isoquinolinone type anticancer agent. Arch Pharm Res. 2001 Aug;24(4):276–80. doi: 10.1007/bf02975091.
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