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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 1-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-4-iodobenzene

HRID 412846
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HRID 412846 반응식
[C:1]([Si:5](Cl)([CH3:7])[CH3:6])([CH3:4])([CH3:3])[CH3:2].[I:9][C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1.O>CN(C)C=O>[I:9][C:10]1[CH:15]=[CH:14][C:13]([O:16][Si:5]([CH3:7])([CH3:6])[C:1]([CH3:4])([CH3:3])[CH3:2])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 108944-IodophenolHCID 28928tert-Butyldimethylsilyl chloride

생성물 1

HCID 148035271-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-4-iodobenzene수율 83.7%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

387 mg of irdidazole and 411 mg of tertbutyldimethylsilyl chloride is added at ambient temperature and under an inert atmosphere to 500 mg of para-iodo-phenol in 4 ml of dimethylformamide and the mixture is maintained under agitation for 15 hours at ambient temperature then for 1 hour at 40° C. The reaction medium is poured into water, and the aqueous phase is extracted with dichloromethane. The organic phase is then dried and evaporated under reduced pressure. In this way 636 mg of expected product is obtained.

후처리

  1. extractionthe aqueous phase is extracted with dichloromethane
  2. customThe organic phase is then dried
  3. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-3717608e307444c5b74b81a0bbac5090
출처 데이터셋
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06563008B2

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