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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375479생성일: 2026년 10월 24일

Water → (1R*,4aR*,7aR*)-4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole 1-oxide (S)-mandelate

https://huagongshe.com/ko/reaction/375479

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물AcetonitrileHCID 6342—
반응물(S)-mandelic acidHCID 439616—
반응물(-)-4,4-Diphenylperhydrothiopyrano[2,3-c]pyrrole 1-oxideHCID 18995289—
용매Acetonitrile--water (1/1)HCID 18373917—
생성물(1R*,4aR*,7aR*)-4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole 1-oxide (S)-mandelateHCID 13171925119.6%

반응 단계

15.8 g of (S)-(+)-mandelic acid and 750 cm3 of a mixture of acetonitrile and water (99/1 by volume) are added to 32.3 g of (1RS,4aRS,7aRS)-4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole 1-oxide, followed by 5.0 cm3 of water. After making lukewarm, the solution obtained is allowed to stand for 48 hours at room temperature. The crystalline suspension is filtered, and the filtrate, concentrated to dryness, gives a meringue which is taken up in 200 cm3 of the boiling acetonitrile-water mixture. The solution obtained is allowed to stand for about 20 hours at room temperature. The crystals are drained, washed with acetonitrile, dried and then again taken up in 200 cm3 of an acetonitrile-water mixture (98/2 by volume). The resulting solution is allowed to stand for about 20 hours at room temperature. The crystals are drained and dried. 9.4 g of (1R*,4aR*,7aR*)-4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole 1-oxide (S)-(+)-mandelate are obtained; [α]D 20 =+337°(c=0 45; acetic acid)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05484942
출처 데이터셋uspto-grants-1996_01
ORD IDord-582138e39e59410d84c0c27bb8898715
출처 메모uspto-grants-1996_01