돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375492생성일: 2026년 10월 24일

2-Methoxyphenylacetic acid → (4aRS,7aRS)-4,4-diphenyl-6-[(2-methoxyphenyl)acetyl]perhydrothiopyrano[2,3-c]pyrrole

https://huagongshe.com/ko/reaction/375492

반응식

참여 물질

역할이름HCID투입량
반응물2-Methoxyphenylacetic acidHCID 7134—
반응물TriethylamineHCID 8471—
반응물(4aRS,7aRS)4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole hydrochlorideHCID 67745331—
용매DichloromethaneHCID 6344—
생성물(4aRS,7aRS)-4,4-diphenyl-6-[(2-methoxyphenyl)acetyl]perhydrothiopyrano[2,3-c]pyrroleHCID 6774534692.6%

반응 조건

온도0 °C

반응 단계

1.13 g of N,N'-carbonyldiimidazole are added to a solution, cooled to 0° C., of 1.16 g of 2-methoxyphenylacetic acid in 20 cm3 of dry dichloromethane. The mixture is stirred for 40 minutes at 0° C. and then a solution of 2.15 g of (4aRS,7aRS)4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole hydrochloride and 0.9 cm3 of triethylamine in 20 cm3 of dichloromethane is added. The reaction mixture is stirred for one hour at 0° C. and is then washed with a saturated aqueous solution of sodium hydrogen carbonate. The organic phase is dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The solid obtained is washed with 30 cm3 of ethyl ether and 30 cm3 of diisopropyl oxide and it is then dried under reduced pressure (2.7 kPa). 2.66 g of (4aRS,7aRS)-4,4-diphenyl-6-[(2-methoxyphenyl)acetyl]perhydrothiopyrano[2,3 -c]pyrrole are obtained in the form of a white solid; melting point 172° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05484942
출처 데이터셋uspto-grants-1996_01
ORD IDord-2680172248a14bcda158531c8b039243
출처 메모uspto-grants-1996_01