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Hydrochloric Acid → 1-(2-Hydroxy-5-tetradecylphenyl)-1-hexanone

HRID 329982
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인쇄 미리보기

반응식

HRID 329982 반응식
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[CH:11][CH:10]=1)(=O)CCCCC.[Cl-].[Al+3].[Cl-].[Cl-].Cl>CCOCC>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[CH:13][C:14]=1[C:9](=[O:8])[CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 6451240Aluminum(III) ChlorideHCID 14819667Hexanoic acid, 4-tetradecylphenyl ester

생성물 1

HCID 142562081-(2-Hydroxy-5-tetradecylphenyl)-1-hexanone수율 170.1%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a melted liquid of 38.8 g of hexanoic acid, 4-tetradecylphenyl ester at 80°-95° C. was added 26.67 g of aluminum chloride in small portions over a period of 2 hours. This mixture was heated for an additional hour, then allowed to cool, diluted with ether and poured onto ice containing 10 ml of concentrated hydrochloric acid. The organic layer was washed with water, dried and the solvent evaporated. The residue was chromatographed on silica gel, eluting with hexane:ethyl acetate (50:1), giving 33 g of the desired compound, mp 41°-42° C.

후처리

  1. temperatureThis mixture was heated for an additional hour
  2. temperatureto cool
  3. washThe organic layer was washed with water
  4. customdried
  5. customthe solvent evaporated
  6. customThe residue was chromatographed on silica gel
  7. washeluting with hexane:ethyl acetate (50:1)

출처 및 근거

ORD 기록
ord-2d7e0d61cb3149078cf21561950acfee
출처 데이터셋
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04894367

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