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Acetate → 1-(2-Hydroxy-4-tetradecylphenyl)ethanone

HRID 703338
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HRID 703338 반응식
[CH2:1]([C:15]1[CH:16]=[C:17]([OH:21])[CH:18]=[CH:19][CH:20]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].[C:22]([O-])(=[O:24])[CH3:23].[Cl-].[Al+3].[Cl-].[Cl-]>CCOCC>[OH:21][C:17]1[CH:16]=[C:15]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH:20]=[CH:19][C:18]=1[C:22](=[O:24])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 175AcetateHCID 6451240Aluminum(III) ChlorideHCID 144404953-Tetradecylphenol

생성물 1

HCID 142562101-(2-Hydroxy-4-tetradecylphenyl)ethanone

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A 20 g portion of 3-tetradecylphenol, acetate was heated at 110° C. and 8.4 g of aluminum chloride was added in portions over a 3 hour period. The mixture was allowed to cool, then diluted with ether, poured onto ice containing 10 ml of concentrated hydrochloic acid and extracted several times with ether. The ether extracts were combined, washed with water, brine and dried. The crude material was chromatographed on silica gel, eluting with hexane:ethyl acetate (50:1), giving 15.8 g of the desired compound, mp 45°-46° C.

후처리

  1. temperatureto cool
  2. additionpoured onto ice containing 10 ml of concentrated hydrochloic acid
  3. extractionextracted several times with ether
  4. washwashed with water, brine
  5. customdried
  6. customThe crude material was chromatographed on silica gel
  7. washeluting with hexane:ethyl acetate (50:1)

출처 및 근거

ORD 기록
ord-7a35c7be91ee4a0bbbdcf8ba8e91b474
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04981989

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