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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1660367생성일: 2026년 10월 24일

Triethanolamine → 1-[2-(Ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine]

https://huagongshe.com/ko/reaction/1660367

반응식

참여 물질

역할이름HCID투입량
반응물TriethanolamineHCID 7618—
반응물Ethyl chloroformateHCID 10928—
반응물1-(2-Aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochlorideHCID 12801598—
용매ChloroformHCID 6212—
생성물1-[2-(Ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine]HCID 12801608—

반응 단계

A slurry of 10.36 g of 1-(2-aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochloride of Example 1b in 60 ml of chloroform is treated portionwise with 12.3 ml of triethanolamine. The resulting mixture is cooled in an ice bath and treated dropwise over 40 minutes with a solution of 2.7 ml of ethyl chloroformate in 20 ml of chloroform. After stirring at room temperature for 1 hour, an additional 3.0 ml of ethyl chloroformate is added and the mixture is permitted to stand 16 hours. The product is washed thrice with water, brine, dried over anhydrous sodium sulfate, concentrated and pumped on under high vacuum to give a crude carbamate. Chromatography on silica gel (100 g) using ether-methylene chloride affords an oil. The material crystallizes on prolonged standing to yield 1-[2-(ethoxycarbonyl)aminophenyl]-1'-methylspiro[indoline-3,4'-piperidine], mp 99.5°-101.0° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04307235
출처 데이터셋uspto-grants-1981_12
ORD IDord-32ed2725ab6a472288674baea068fbd2
출처 메모uspto-grants-1981_12