CAS: 2425-74-3; N-Tert-Butylformamide

相似化合物

762-84-5 1118-69-0 1118-12-3

上下游产品

CAS号124-38-9 二氧化碳 | CAS号75-64-9 叔丁胺 | CAS号64-18-6 甲酸 | CAS号13987-61-6 2-Methyl-N-meth... | CAS号77287-34-4 甲亚胺酸 | CAS号201230-82-2 carbon monoxide | CAS号107-31-3 甲酸甲酯 | CAS号773837-37-9 sodium cyanide | CAS号75-65-0 叔丁醇 | CAS号74-90-8 氢氰酸 | CAS号51609-06-4 N-叔丁基环己胺 | CAS号75-64-9 叔丁胺 | CAS号5894-65-5 N-(叔-丁基)苯甲酰胺 | CAS号103202-88-6 methyl N-tert-b... | CAS号14610-37-8 N-甲基-叔丁基胺 | CAS号23314-06-9 N'-叔-丁基-N,N-二甲基甲脒 | CAS号37486-48-9 N,N-ditert-buty... | CAS号10017-37-5 叔丁基氯化铵 | CAS号88842-41-5 N-tert-butyl-N-... | CAS号89656-25-7 N-tert-butyl-1-...

📜叔丁基亚甲基胺置于sodium Hydroxide,双氧水体系中,用 水 用作溶剂,以89%的收率获得n-叔丁基甲胺
参考文献:Process For Producing N-Monosubstituted Formamides
标题:Process For Producing N-Monosubstituted Formamides
摘要:具有以下公式的n-单取代甲酰胺:##equ1##其中r代表可选择地取代的脂肪族,环脂族或芳香族基团;通过将具有以下公式的甲醛二亚胺:H.Sub.2 C = N--R,其中r如上所定义;或具有以下公式的六氢三唑:##equ2##其中r如上所定义,与过氧化氢反应制备.反应通常在约0oc至约100oc的温度范围内进行.

专利信息

专利号:US-10364220-B2
优先权日:2012-12-21
标题:Synthesis of succinimides and quaternary ammonium ions for use in making molecular sieves
发明人：SCHMITT KIRK D; ZUSHMA STEPHEN; BURTON ALLEN W
权利人:EXXONMOBIL CHEMICAL PATENTS INC
摘要:The present invention relates to the synthesis of succinimides, in particular to a method for the synthesis of a succinimide compound, comprising the step of reacting an alkyne, with carbon monoxide and ammonia or an amine, in the presence of an iron catalyst, wherein the reaction is carried out in an amine liquid phase and/or in the absence of an ether solvent. The succinimides may be reduced to quaternary ammonium cations which may be used as structure directing agents in the synthesis of molecular sieves.

专利号:US-10253153-B2
优先权日:2015-04-24
标题 :Linker and support for solid phase synthesis of nucleic acid, and production method of nucleic acid using said support
发明人：MAETA ERI; MORI KENJIRO; HORIE SHOHEI; ITO TAKAHIKO; SAITO SHOICHIRO; NAGAO RYUHEI
权利人:NITTO DENKO CORP
摘要:The present invention provides a linker for solid phase synthesis of nucleic acid, which consists of a compound represented by the formula (I) or the formula (II), a support for solid phase synthesis of nucleic acid, which has a structure represented by the formula (III), and a production method of a nucleic acid, which uses the support: n nwherein each symbol is as defined in the SPECIFICATION.

专利号:US-4879389-A
优先权日:1986-06-25
标题:Chiral phosphinopyrrolidine compounds and their use for asymmetric synthesis of optically active compounds
发明人：ACHIWA KAZUO
权利人:ACHIWA KAZUO
摘要:New chiral phosphinopyrrolidine compounds of the general formula: (I) or (I') wherein R1 is a hydrogen atom, -COR, -COOR, -CONHR or -SO2-R where R is an alkyl or aryl group, R2 and R3 each represents independently an aryl group which may have a substituent or substituents, and R4 and R5 each represents independently an aliphatic or cycloaliphatic hydrocarbyl group which may have a substituent or substituents, as well as the use of these compounds as ligand for a metal complex catalyst for asymmetric synthesis of optically active compounds. The new chiral phosphinopyrrolidine compounds are useful ligands which attain both of high optical yield and high reaction efficiency in catalytic asymmetric reduction.

专利号:US-8729277-B2
优先权日:2009-04-06
标 题:Processes for the synthesis of gamma nitrocarbonyl and gamma dicarbonyl compounds and their pyrrole derivatives
发明人：YANG HU; BARALT EDUARDO J
权利人:YANG HU; BARALT EDUARDO J; CHEVRON PHILLIPS CHEMICAL CO
摘要:The present invention discloses processes for producing γ-nitrocarbonyl and γ-dicarbonyl compounds, which can be precursors in the synthesis of pyrrole compounds. A process for producing pyrroles such as 2,5-dimethylpyrrole, and structurally similar pyrrole compounds, is also disclosed.

专利号:US-5633373-A
优先权日:1989-07-07
标 题 :Enantioselective synthesis of antifolates
发明人：BARNETT CHARLES J; WILSON THOMAS M
权利人:LILLY CO ELI
摘要:A process and intermediates for the enantioselective synthesis of 5,10-dideaza-5,6,7,8-tetrahydrofolic acid are disclosed.

专利号:US-7470792-B2
优先权日:2002-09-13
标题:Process for the preparation of epothilone derivatives, new epothilone derivatives as well as new intermediate products for the process and the methods of preparing same
发明人：KOCH GUIDO; LOISELEUR OLIVIER
权利人:NOVARTIS AG
摘要:The present invention provides a synthesis for the preparation of epothilone derivatives of formula 9 n nwherein R1 is methyl, and R2 is an unsubstituted or substituted aryl; an unsubstituted or substituted heteroaryl; or an unsubstituted or substituted heterocyclic radical fused to a benzene nucleus; and salts thereof, and intermediates for the synthesis of a compound of formula 9.