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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Imidazole → ((5-Bromo-4-methyl-1,3-dihydroisobenzofuran-1-yl)oxy)(tert-butyl)dimethylsilan

HRID 1848557
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HRID 1848557 반응식
[Si:1](Cl)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[Br:9][C:10]1[C:11]([CH3:20])=[C:12]2[C:16](=[CH:17][CH:18]=1)[CH:15]([OH:19])[O:14][CH2:13]2.N1C=CN=C1>C(Cl)Cl>[Br:9][C:10]1[C:11]([CH3:20])=[C:12]2[C:16](=[CH:17][CH:18]=1)[CH:15]([O:19][Si:1]([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2])[O:14][CH2:13]2
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참가 물질

5

반응물 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 867095385-Bromo-4-methyl-1,3-dihydroisobenzofuran-1-ol

생성물 1

HCID 86709540((5-Bromo-4-methyl-1,3-dihydroisobenzofuran-1-yl)oxy)(tert-butyl)dimethylsilan

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of TBS-Cl (3.63 g, 24.10 mmol) in methylene chloride (15 mL) was added to a solution of 5-bromo-4-methyl-1,3-dihydroisobenzofuran-1-ol (2.76 g, 12.1 mmol) and imidazole (1.72 g, 25.3 mmol) in methylene chloride (80 mL) at 0° C., the resulting solution was stirred at rt overnight. The mixture was partitioned between DCM and water, the water phase was extracted with methylene chloride and the combined organic phase was dried over sodium sulfate then concentrated, and the residue was purified on silica gel column using ethyl acetate/hexane to give the title compound. LC/MS: (M−131)+: 210.91; 212.91.

후처리

  1. customThe mixture was partitioned between DCM and water
  2. extractionthe water phase was extracted with methylene chloride
  3. dry with materialthe combined organic phase was dried over sodium sulfate
  4. concentrationthen concentrated
  5. customthe residue was purified on silica gel column

출처 및 근거

ORD 기록
ord-09803a9fe95640cf8fce31b9351e7633
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952166B2

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