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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375442생성일: 2026년 10월 24일

Triethylamine → (3aRS,4RS,5RS,7aRS)-7,7-diphenyl-4-(2-methoxyphenyl)-2-(2-methoxyphenyl)-acetylperhydroisoindole-4,5-diol

https://huagongshe.com/ko/reaction/375442

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-(2-Methoxyphenyl)acetyl chlorideHCID 179502—
반응물7,7-Diphenyl-4-(2-methoxyphenyl)-perhydroisoindole-4,5-diol hydrochlorideHCID 67719297—
용매DichloromethaneHCID 6344—
생성물(3aRS,4RS,5RS,7aRS)-7,7-diphenyl-4-(2-methoxyphenyl)-2-(2-methoxyphenyl)-acetylperhydroisoindole-4,5-diolHCID 6771904177.5%

반응 조건

온도0 °C

반응 단계

4.2 cm3 of triethylamine and then 2.4 g of (2-methoxyphenyl)acetic acid chloride in 50 cm3 of dichloromethane are added to a solution of 4.5 g of (3aRS,4RS,5RS,7aRS)-7,7-diphenyl-4-(2-methoxyphenyl)perhydroisoindole-4,5-diol hydrochloride in 100 cm3 of dichloromethane, cooled to 0° C. The reaction mixture is stirred at room temperature for 90 minutes; it is washed with twice 10 cm3 of water, and is dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The solid which has crystallized is taken up in. 100 cm3 of diisopropyl ether and then filtered off and washed with 50 cm3 of a saturated solution of sodium bicarbonate and then 50 cm3 of diisopropyl ether. 4.35 g of (3aRS,4RS,5RS,7aRS)-7,7-diphenyl-4-(2-methoxyphenyl)-2-(2-methoxyphenyl)- acetylperhydroisoindole-4,5-diol are obtained in the form of a light beige solid which melts at 278° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05484804
출처 데이터셋uspto-grants-1996_01
ORD IDord-bc91623981414751a493d75015c2b359
출처 메모uspto-grants-1996_01