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Imidazole → 4-(4-Methylphenyl)butyl tert-butyldimethylsilyl ether

HRID 1516081
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HRID 1516081 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][CH2:11][OH:12])=[CH:4][CH:3]=1.N1C=CN=C1.[Si:18](Cl)([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19]>CN(C=O)C>[Si:18]([O:12][CH2:11][CH2:10][CH2:9][CH2:8][C:5]1[CH:6]=[CH:7][C:2]([CH3:1])=[CH:3][CH:4]=1)([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19]
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참가 물질

5

반응물 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 1040094-(4-Methylphenyl)butanol

생성물 1

HCID 596786264-(4-Methylphenyl)butyl tert-butyldimethylsilyl ether

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

4-(4-Methylphenyl)butanol (0.5 g, 3.04 mmol) is dissolved in 5 ml DMF and to it is added imidazole (310 mg, 4.56 mmol) and tert-butyldimethylsilyl chloride (685 mg, 4.56 mmol). The reaction is stirred for 4 hrs after which it is extracted in ethyl acetate and washed with water to remove all DMF. The organic layer is then dried and concentrated. The crude mixture is then purified by flash chromatography using a mixture of ethyl acetate-hexanes as the eluting medium to afford the above mentioned product.

후처리

  1. extractionis extracted in ethyl acetate
  2. washwashed with water
  3. customto remove all DMF
  4. customThe organic layer is then dried
  5. concentrationconcentrated
  6. customThe crude mixture is then purified by flash chromatography
  7. additiona mixture of ethyl acetate-hexanes as the eluting medium
  8. customto afford the

출처 및 근거

ORD 기록
ord-7367dbe50b454478bebd581218e43461
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08226929B2

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