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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375438생성일: 2026년 10월 24일

Triethylamine → HCID 56978006, 화합물

https://huagongshe.com/ko/reaction/375438

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Indoleglyoxylyl chlorideHCID 89952—
반응물(3aS,4S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)perhydroisoindol-4-ol hydrochlorideHCID 70218598—
용매DichloromethaneHCID 6344—
생성물HCID 56978006HCID 5697800697.3%

반응 단계

A solution of 0.43 g of 2-(3-indolyl)-2-oxoacetyl chloride in 20 cm3 of dry dichloromethane and then a solution of 0.6 cm3 of triethylamine in 5 cm3 of dry dichloromethane are added in succession to a suspension of 0.96 g of (3aS,4S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)perhydroisoindol-4-ol hydrochloride in 25 cm3 of dry dichloromethane at room temperature, while stirring. The reaction mixture is stirred at this temperature for 24 hours, subsequently diluted with 200 cm3 of dichloromethane, washed with 100 cm3 of an aqueous 1N solution of sodium hydroxide and with 50 cm3 of an aqueous saturated solution of sodium chloride, and is dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a Merck silica gel column (particle size 0.04-0.06 mm, diameter 2.5 cm, height 1 cm) by eluting under a pressure of 0.4 bar of nitrogen with a mixture of 1,2-dichloroethane and methanol (70/30 by volume) and collecting fractions of 15 cm3. Fractions 2 to 9 are combined and concentrated to dryness under reduced pressure (2.7 kPa). 1.15 g of (3aS,4S,7aS)-7,7-diphenyl-2-[2-oxo-2-(3-indolyl)acetyl]-4-(2-methoxyphenyl)perhydroisoindol-4-ol are obtained in the form of an orange foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05484804
출처 데이터셋uspto-grants-1996_01
ORD IDord-06c4dca4b5eb4defb8c1dbf6a287d814
출처 메모uspto-grants-1996_01