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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24498생성일: 2026년 10월 25일

Acetic Acid → 3-(2-ethoxycarbonylethyl)-4,5,6,7-tetrahydro-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/24498

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium AcetateHCID 517045—
반응물Propanedioic acid, 2-amino-, 1,3-diethyl ester, hydrochloride (1:1)HCID 3084143—
반응물4-(2-Morpholin-4-ylcyclohex-1-enyl)-4-oxo-butyric acid ethyl esterHCID 10589972—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물3-(2-ethoxycarbonylethyl)-4,5,6,7-tetrahydro-1H-indole-2-carboxylic acid ethyl esterHCID 10803658109.6%

반응 조건

온도50 °C

반응 단계

Crude 4-(2-morpholin-4-ylcyclohex-1-enyl)-4-oxo-butyric acid ethyl ester (454 g), 398 g of diethyl aminomalonate hydrochloride, 162 g of sodium acetate and 350 mL of glacial acetic acid were heated to 108° C. over 30 minutes. The mixture was held at 100-108° C. for 2 hours and then cooled to about 50° C. in a water bath. Water (2500 mL) and 700 mL of ethyl acetate were added. The ethyl acetate layer was separated and washed three times with brine, twice with saturated sodium bicarbonate solution and once with brine. The solution was dried over anhydrous sodium sulfate, and the ethyl acetate was removed using a rotary evaporator to give 494 g (105% yield) of crude 3-(2-ethoxycarbonylethyl)-4,5,6,7-tetrahydro-1H-indole-2-carboxylic acid ethyl ester as an oil. The crude mixture was chromatographed on a silica gel column using a 1:10 mixture of ethyl acetate:hexane as the eluent to give 122.1 g of pure 3-(2-ethoxycarbonylethyl)-4,5,6,7-tetrahydro-1H-indole-2-carboxylic acid ethyl ester as a low melting solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-2b6b5064704b440e8c317f0eb94c8d1c
출처 메모uspto-grants-2005_02