2-Phenylethyl Acetate → 4-Octanoylphenethyl acetate

HRID 862822노트

반응식

HRID 862822 반응식
[Cl-].[Al+3].[Cl-].[Cl-].[C:5]([O:8][CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)(=[O:7])[CH3:6].[C:17](Cl)(=[O:27])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24]CC>ClC(Cl)C>[C:5]([O:8][CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([C:17](=[O:27])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])=[CH:13][CH:12]=1)(=[O:7])[CH3:6]

참가 물질

5

반응물 3

HCID 76542-Phenylethyl AcetateHCID 66982Decanoyl chlorideHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 217075284-Octanoylphenethyl acetate수율 40.3%

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매

실험 절차

Aluminum chloride (111.8 g) was added to dichloroethane (500 ml) in a stream of nitrogen and the mixture was stirred at room temperature. Then, phenethyl acetate (91.8 g) and decanoyl chloride (100 g) were dropwise added thereto under ice-cooling and the mixture was stirred at room temperature overnight. The reaction mixture was poured into ice water and extracted with diethyl ether. The ether layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled away and the residue was purified by silica gel column chromatography (eluent; ethyl acetate:hexane=1:20) to give 61.3 g of the subject compound (yield 38%) as an oily substance.

후처리

  1. temperatureunder ice-cooling
  2. stirringthe mixture was stirred at room temperature overnight
  3. extractionextracted with diethyl ether
  4. washThe ether layer was washed with saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationThe solvent was distilled away
  7. customthe residue was purified by silica gel column chromatography (eluent; ethyl acetate:hexane=1:20)

출처 및 근거

ORD 기록
ord-d7279e5b6ba940f4853ff27a294eee36
출처 데이터셋
uspto-grants-1998_02
특허 번호
US05719176

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