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Imidazole → HCID 13470490, 화합물

HRID 462385
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HRID 462385 반응식
[Cl:1][CH2:2][CH2:3][CH2:4]/[CH:5]=[CH:6]\[CH2:7][OH:8].N1C=CN=C1.[Si:14](Cl)([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15]>CN(C)C=O>[Si:14]([O:8][CH2:7]/[CH:6]=[CH:5]\[CH2:4][CH2:3][CH2:2][Cl:1])([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 13445192HCID 13445192, 화합물

생성물 1

HCID 13470490HCID 13470490, 화합물수율 92.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

98 g of 6-chlorohex-2Z-en-1-ol was dissolved in 250 ml of dimethylformamide and treated with 68 g of imidazole and 113 g of t-butyldimethylsilyl chloride. After stirring 1.5 hours at room temperature, the reaction mixture was poured into ice water and extracted twice with 300 ml of ether. The ethereal solution was washed with 5% hydrochloric acid, aqueous sodium bicarbonate and brine. After drying over potassium carbonate the solvent was evaporated and the residue distilled to give 168.1 g of 6-chlorohex-2Z-en-1-ol t-butyldimethylsilyl ether, bp 95°-100° C./0.4 mm.

후처리

  1. extractionextracted twice with 300 ml of ether
  2. washThe ethereal solution was washed with 5% hydrochloric acid, aqueous sodium bicarbonate and brine
  3. dry with materialAfter drying over potassium carbonate the solvent
  4. customwas evaporated
  5. distillationthe residue distilled

출처 및 근거

ORD 기록
ord-1cd5dcebebec42488293ffe2e70f7379
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04515727

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