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HRID 241721생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/241721

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물BenzocaineHCID 2337—
반응물Ethyl (methylthio)acetateHCID 78199—
반응물Tert-Butyl hypochloriteHCID 521297—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물Ethyl 3-methylsulphanyl-2-oxo-2,3-dihydro-1H-indole-5-carboxylateHCID 12351489—

반응 조건

온도-50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653073B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-84946997eaee4cdebaa0e7d71de82a98
출처 메모uspto-grants-2014_02