- 英文名称2-(4-Bromobutyl)Benzo[d][1,3,2]Dioxaborole
- 中文名称2-(4-溴丁基)苯并[d][1,3,2]二氧杂环戊烷
- IUPAC名称2-(4-bromobutyl)benzo[d][1,3,2]dioxaborole
- 其它别名2-(4-溴丁基)-1,3,2-苯并二氧硼烷; 2-(4-Bromobutyl)-1,3,2-Benzodioxaborole
- CAS编号142172-51-8
- MFCD编号:MFCD01863716
- EINECS号:627-967-7
- 分子式:C10H12BBrO2分子量:254.92
- 产品CID: 646162
- 产品分类有机原料→分子砌块→芳杂环类化合物→其它芳杂环类化合物
相似化合物
274-07-7 55718-76-8 40218-49-3欧盟法规
ECHA物质C&L通报上下游产品
CAS号5162-44-7 4-溴-1-丁烯 | CAS号274-07-7 儿茶酚硼烷 | CAS号13633-25-5 4-苯基-1-丁基溴📜4-溴-1-丁烯,儿萘酚硼烷 反应 18.0H,以88%的收率获得2-(4-溴丁基)-1,3,2-苯并二氧杂戊硼烷
参考文献:新型α-链含硼酸酯的前列腺素的合成
标题:新型α-链含硼酸酯的前列腺素的合成
摘要:已经合成了一类新的在α链上含有硼酸酯的前列腺素.合成中的关键步骤是制备含硼酸酯的叶立德和随后使用该叶立德的wittig反应.
Doi:10.1016/s0040-4039(00)00973-4
海关参考信息
- 2907210001-间苯二酚
2903399020-溴甲烷
2908199090-其他酚的卤化衍生物
2908999090-其他酚的硝化衍生物 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:WO-2016037298-A1
优先权日:2014-09-11
标题 :Method for the enantioselective synthesis of 2(s)-amino-6-boronohexanoic acid (abh) and purification thereof
发明人:PREITE MARCELO DANIEL; MANRIQUEZ MUJICA JUAN MANUEL; CORREA VARGAS JORDAN MAURICIO; ITURRIAGA AGUERA RODRIGO MANUEL; CASANELLO TOLEDO PAOLA CECILIA; KRAUSE LEYTON BERNARDO JAVIER
权利人:UNIV PONTIFICIA CATOLICA CHILE
摘要:The invention relates to a method for the enantioselective synthesis and purification of 2(S)-amino-6-boronohexanoic acid (ABH) and the preparation of the corresponding synthetic intermediates. The method comprises the preparation of ABH from BPB-Ni-Gly, which is treated with a strong base in a suitable solvent, and is made to react with 2-(4-lower bromoalkyl)benzo[d] [1,3,2]dioxaborol, where the lower alkyl is an alkyl with between 1 and 6 carbon atoms, preferably 2-(4- bromo-butyl)benzo[d][1,3,2]dioxaborol, while stirring, in a nitrogen atmosphere and with a cryogenic bath at a low temperature (-50°C), in order to then permit same to reach ambient temperature, removing the cryogenic bath, before neutralising in aqueous medium with a weak organic acid, and extracting with dichloromethane, drying the resulting organic extract which is subsequently filtered and vacuum evaporated. The resulting alkylated complex is dissolved in a C1-C5 alcohol, adding a hydrochloric acid, refluxing in a nitrogen atmosphere, and is subsequently cooled to ambient temperature, and concentrated in order to achieve the precipitation of (S)-2-[N-(N'- benzylprolyl) amino]benzophenone (BPB), as the hydrochloride salt, filtering and extracting with dichloromethane, and after dissolving the aqueous phase of the filtrate in water, it is treated with ammonia concentrated to pH 9, and once again extracted with dichloromethane, the ammoniacal aqueous phase being vacuum evaporated until dry, in order to produce crude ABH, as the ammonium salt, which is subsequently purified by means of ion-exchange chromatography. The invention also relates to a method for preparing the Gly-Ni-BPB complex, 2-(4- bromo-butyl)benzo[d][1,3,2]dioxaborol, which is used as an alkylating agent in the form of a borate side chain, and (S)-N- benzylproline (BP).