홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Phosphorus sulfide (P2S5) → 2H-Pyran-2-thione, 4,6-diphenyl-

HRID 1165285
노트
인쇄 미리보기

반응식

HRID 1165285 반응식
[C:1]1([C:7]2[CH:12]=[C:11]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[O:10][C:9](=O)[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:21]>C1C=CC=CC=1>[C:1]1([C:7]2[CH:12]=[C:11]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[O:10][C:9](=[S:21])[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14817Phosphorus sulfide (P2S5)HCID 2966854,6-diphenyl-2H-pyran-2-one

생성물 1

HCID 1861062H-Pyran-2-thione, 4,6-diphenyl-수율 134.2%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

Under an inert atmosphere, 2.1 g of the product of Step A 45 ml of benzene and 7.5 g of phosphorus pentasulfide were mixed together and refluxed under inert atmosphere for 5 hours. Then the supernatant solution was decanted hot and concentrated to dryness by distilling under reduced pressure. This operation was repeated hot on the reaction medium four times, each time with 30 ml of benzene. The concentrates were put together and dried under a good vacuum to obtain 3 g of product which was chromatographed on silica and eluted with methylene chloride to obtain 2 g of the product sought melting at 122°-123° C.

후처리

  1. temperaturerefluxed under inert atmosphere for 5 hours
  2. customThen the supernatant solution was decanted hot
  3. concentrationconcentrated to dryness
  4. distillationby distilling under reduced pressure
  5. customdried under a good vacuum

출처 및 근거

ORD 기록
ord-4de36a03eb69437e9c456d72aecbb8af
출처 데이터셋
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04908359

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트