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Hexane → 1-(3-Benzyloxyphenyl)-1,1-dimethylheptane

HRID 1153893
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HRID 1153893 반응식
[CH2:1]([Mg]Br)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[CH3:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].[CH2:15]([O:22][C:23]1[CH:24]=[C:25]([C:29](Cl)([CH3:31])[CH3:30])[CH:26]=[CH:27][CH:28]=1)C1C=CC=CC=1.[Cl-].[NH4+]>CCOCC>[CH2:15]([O:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([C:29]([CH3:30])([CH3:31])[CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])[CH:24]=1)[C:11]1[CH:10]=[CH:9][CH:14]=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8058Hexane2회HCID 25517Ammonium ChlorideHCID 133680332-(3-Benzyloxyphenyl)-2-chloropropaneHCID 178444609HCID 178444609, 화합물

생성물 1

HCID 130526961-(3-Benzyloxyphenyl)-1,1-dimethylheptane수율 35%

시약·촉매·용매 1

HCID 3283
Diethyl Ether
용매

실험 절차

To a 0° C. mixture of 10.1 mmole of n-hexyl magnesium bromide in 5 ml. of hexane is added dropwise a solution of 2.0 g. (7.69 mmole) of 2-(3-benzyloxyphenyl)-2-chloropropane in 14 ml. of hexane. The reaction mixture is stirred 5 minutes longer and then added to 500 ml. of saturated ammonium chloride and 300 ml. ether. The organic extract is dried over magnesium sulfate and evaporated to an oil. The oil is purified via column chromatography on 150 g. of silica gel eluted with hexane to yield 841 mg. (35%) of the title compound as an oil.

후처리

  1. additionadded to 500 ml
  2. extractionThe organic extract
  3. dry with materialis dried over magnesium sulfate
  4. customevaporated to an oil
  5. customThe oil is purified via column chromatography on 150 g
  6. washof silica gel eluted with hexane
  7. customto yield 841 mg

출처 및 근거

ORD 기록
ord-a4f7fb656a924800ae4e35e974701db3
출처 데이터셋
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04486609

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