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

p-Toluenesulfonic acid monohydrate → HCID 70020197, 화합물

HRID 1357502
노트
인쇄 미리보기

반응식

HRID 1357502 반응식
O.C1(C)C=CC(S(O)(=O)=O)=CC=1.[C:13]([O:21][C@H:22]1[C@@H:27]2[O:28]C(C)(C)[O:30][C@@H:26]2[CH:25]=[C:24]([C:33]([O:35][CH3:36])=[O:34])[CH2:23]1)(=[O:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>CO>[C:13]([O:21][C@H:22]1[C@H:27]([OH:28])[C@H:26]([OH:30])[CH:25]=[C:24]([C:33]([O:35][CH3:36])=[O:34])[CH2:23]1)(=[O:20])[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 91573293HCID 91573293, 화합물

생성물 1

HCID 70020197HCID 70020197, 화합물수율 54%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Para-toluenesulfonic acid monohydrate (100 mg, 0.526 mmol) was added to a room temperature solution of Example 13D in methanol (50 mL). After stirring overnight, the reaction mixture was concentrated and the concentrate was purified by flash chromatography using ethyl acetate to afford 0.90 g (54%) of the desired product as a colorless oil.

후처리

  1. concentrationthe reaction mixture was concentrated
  2. customthe concentrate was purified by flash chromatography

출처 및 근거

ORD 기록
ord-4a8bb7ea683a48aa81c6a55d6a071bbc
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06593314B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트