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HRID 44266作成日:2026年10月24日

Hydrochloric Acid → Ethyl 3-methylsulphanyl-2-oxo-2,3-dihydro-1H-indole-5-carboxylate

https://huagongshe.com/ja/reaction/44266

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物BenzocaineHCID 2337—
反応物Ethyl (methylthio)acetateHCID 78199—
反応物Tert-Butyl hypochloriteHCID 521297—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物Ethyl 3-methylsulphanyl-2-oxo-2,3-dihydro-1H-indole-5-carboxylateHCID 12351489—

反応条件

温度-50 °C

反応手順

To a solution of ethyl 4-amino-benzoate (40.0 g) in DCM (900 ml) at −60° C. there is added, dropwise, ethyl(methylsulphanyl)acetate (34.5 ml) under a nitrogen atmosphere. 29.0 g of tBuOCl are then added, dropwise, to the reaction mixture over 25 minutes, maintaining the temperature between −60° C. and −55° C. After stirring for one hour at −50° C., triethylamine (15.4 ml) is added dropwise. The reaction mixture is brought to 0° C. and then aqueous 3M HCl solution (485 ml) is added dropwise. After stirring for 12 hours at ambient temperature, the phases are separated and the organic phase is washed successively with aq. 2M HCl solution, water and then sat. aqueous NaCl solution. The organic phase is dried over sodium sulphate, filtered and evaporated to dryness. The residue obtained is taken up in ether. The crystals obtained are filtered off, washed with ether and dried in vacuo to yield the title product, which is used directly in the next Step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541412B2
出典データセットuspto-grants-2013_09
ORD IDord-506deeb5f54946d7a3c2fa62f0204408
出典メモuspto-grants-2013_09