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

Diphenyl carbonate → 3-(4-Methoxybenzyl)thiazolidin-2-one

HRID 2108005
노트
인쇄 미리보기

반응식

HRID 2108005 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][NH:10][CH2:11][CH2:12][SH:13])=[CH:5][CH:4]=1.[C:14](=O)(OC1C=CC=CC=1)[O:15]C1C=CC=CC=1>C(O)C>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][N:10]2[CH2:11][CH2:12][S:13][C:14]2=[O:15])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7597Diphenyl carbonateHCID 14306201N-(4-methoxybenzyl)-cysteamine

생성물 1

HCID 230450983-(4-Methoxybenzyl)thiazolidin-2-one수율 32.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution containing 4.53 g (0.025 mol) of N-(4-methoxyphenylmethyl)-cysteamine and 5.35 g (0.025 mol) of diphenyl carbonate in 25 ml of ethanol is refluxed under nitrogen for 24 hours, then evaporated. The residue is taken up in ethyl acetate, washed with 2N sodium hydroxide solution until it becomes free from phenol, then washed with water, dried and evaporated. The residue becomes solid under ether. Thus, 1.82 g (32.6%) of the title compound are obtained, m.p.: 84°-86° C.

후처리

  1. temperatureis refluxed under nitrogen for 24 hours
  2. customevaporated
  3. washwashed with 2N sodium hydroxide solution until it
  4. washwashed with water
  5. customdried
  6. customevaporated

출처 및 근거

ORD 기록
ord-9ef934f1ce8042f59c3b127ca83ef784
출처 데이터셋
uspto-grants-1990_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04937252

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트