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p-Toluenesulfonic acid → 4-(4-Fluorophenyl)-4-methoxycyclohexanone

HRID 2260503
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HRID 2260503 반응식
[CH3:1][O:2][C:3]1([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=2)[CH2:12][CH2:11][C:6]2(OCC[O:7]2)[CH2:5][CH2:4]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>CC(C)=O.C([O-])(O)=O.[Na+]>[F:19][C:16]1[CH:15]=[CH:14][C:13]([C:3]2([O:2][CH3:1])[CH2:4][CH2:5][C:6](=[O:7])[CH2:11][CH2:12]2)=[CH:18][CH:17]=1
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참가 물질

5

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 571381988-(4-Fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol methyl ether

생성물 1

HCID 184002134-(4-Fluorophenyl)-4-methoxycyclohexanone수율 94%

시약·촉매·용매 2

HCID 180Acetone용매HCID 516892Sodium Bicarbonate용매

실험 절차

A solution of 8-(4-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol methyl ether in acetone (200 ml) was stirred for 96 hr with p-toluenesulfonic acid (0.1 g) and the solution diluted with saturated NaHCO3 solution. The mixture was concentrated in vacuo and the residue suspended in water. The mixture was extracted with ether and the ether extracts dried and concentrated in vacuo. The residue was crystallized from hexane to give 4-(4-fluoro-phenyl)-4-methoxycyclohexanone (94%, mp: 57°-59° C.).

후처리

  1. concentrationThe mixture was concentrated in vacuo
  2. extractionThe mixture was extracted with ether
  3. dry with materialthe ether extracts dried
  4. concentrationconcentrated in vacuo
  5. customThe residue was crystallized from hexane

출처 및 근거

ORD 기록
ord-5436c45f73de4809bf78cef6c9659b82
출처 데이터셋
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05478828

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