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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 22018460, 화합물 → HCID 22018435, 화합물

HRID 1368562
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반응식

HRID 1368562 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH:13]([C:15]1[S:19][CH:18]=[N:17][CH:16]=1)[OH:14])[CH:7]=[CH:6]2>ClCCl.[O-2].[O-2].[Mn+4]>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([C:13]([C:15]1[S:19][CH:18]=[N:17][CH:16]=1)=[O:14])[CH:7]=[CH:6]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 22018460HCID 22018460, 화합물

생성물 1

HCID 22018435HCID 22018435, 화합물수율 86.1%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6344Dichloromethane용매

실험 절차

(6-methoxynaphthalen-2-yl)(thiazol-5-yl)methanol (2.0 g) was dissolved in dichloromethane (30 ml). To the solution was added manganese dioxide (6.0 g), and the mixture was stirred at room temperature for 3 h. The mixture was filtered with celite and the cake was rinsed with dichloromethane. The filtrate was concentrated and the obtained residue was recrystallized from ethyl acetate to give the titled compound (1.71 g) as a pale yellow powder.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. filtrationThe mixture was filtered with celite
  2. washthe cake was rinsed with dichloromethane
  3. concentrationThe filtrate was concentrated
  4. customthe obtained residue was recrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-862ad7b7582c4f55b47c009936194fb9
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06573289B1

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