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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 11018798, 화합물 → HCID 10519016, 화합물

HRID 1078506
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인쇄 미리보기

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HRID 1078506 반응식
C[S-].[Li+].CCOCC.CCCCCC.[C:15]([C:19]1[CH:20]=[C:21]([C:26]([CH3:37])=[CH:27][C:28]2[CH:36]=[CH:35][C:31]([C:32]([OH:34])=[O:33])=[CH:30][CH:29]=2)[CH:22]=[CH:23][C:24]=1[OH:25])([CH3:18])([CH3:17])[CH3:16]>CN(C=O)C>[C:15]([C:19]1[CH:20]=[C:21](/[C:26](/[CH3:37])=[CH:27]/[C:28]2[CH:29]=[CH:30][C:31]([C:32]([OH:34])=[O:33])=[CH:35][CH:36]=2)[CH:22]=[CH:23][C:24]=1[OH:25])([CH3:18])([CH3:16])[CH3:17]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11018798HCID 11018798, 화합물HCID 21584099Diethylether hexaneHCID 54246648HCID 54246648, 화합물

생성물 1

HCID 10519016HCID 10519016, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
120 °C

실험 절차

1.84 g of lithium methanethiolate are added to 2 g (5.67 mmol) of the E ester obtained in Example 33(b) in 40 ml of DMF. The reaction mixture is stirred under nitrogen at 120° C. for 4 h. After the same treatment as in Example 8, followed by a chromatography in the ether/hexane eluent (80/20), 1.69 g of a mixture of E and Z isomers of 4-[-2-(3-tert-butyl-4-hydroxyphenyl)propenyl]benzoic acid are isolated in the respective proportions (83:17). A recrystallization from the hexane/ether mixture gives 225 mg of the expected derivative which melts at 209° C.

후처리

  1. customare isolated in the respective proportions (83:17)
  2. customA recrystallization from the hexane/ether mixture
  3. customgives 225 mg of the expected derivative which melts at 209° C.

출처 및 근거

ORD 기록
ord-5af5a44a7ede42a3ac1bf619b190edc3
출처 데이터셋
uspto-grants-1996_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05547983

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