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Dimethylformamide → 3-Formyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane

HRID 66291
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반응식

HRID 66291 반응식
[H-].[Na+].C(S)C.Cl.C[O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]23[CH2:20][CH:19]2[CH2:18][NH:17][CH2:16]3)=[CH:11][CH:10]=1.CN(C)[CH:23]=[O:24]>>[CH:23]([N:17]1[CH2:18][CH:19]2[C:15]([C:12]3[CH:13]=[CH:14][C:9]([OH:8])=[CH:10][CH:11]=3)([CH2:20]2)[CH2:16]1)=[O:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6228Dimethylformamide3회HCID 6343EthanethiolHCID 24758Sodium hydride2회HCID 127198561-(4-Methoxyphenyl)-3-azabicyclo[3.1.0]hexane Hydrochloride

생성물 1

HCID 127198763-Formyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane

실험 절차

To a slurry of 7.2 g (0.15 mol) of sodium hydride (50% oil dispersion) in 170 ml of N,N-dimethylformamide at 0°-5° is added a solution of 10.1 ml of ethanethiol in 85 ml of N,N-dimethylformamide over a 15 minute period. An additional 3.16 g portion of sodium hydride is added followed by 14.4 g of 1-(p-methoxyphenyl)-3-azabicyclo[3.1.0]hexane hydrochloride. After the addition of 40 ml of N,N-dimethylformamide, the mixture is refluxed for 4 hours and the solvent is then removed. The residue is dissolved in 150 ml of water and mineral oil is extracted with ether. The aqueous solution is made acidic with acetic acid and the precipitated crystals are collected by filtration to give 9.8 g of 3-formyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane as tan crystals, m.p. 166°-167°.

후처리

  1. temperaturethe mixture is refluxed for 4 hours
  2. customthe solvent is then removed
  3. dissolutionThe residue is dissolved in 150 ml of water
  4. extractionmineral oil is extracted with ether
  5. filtrationthe precipitated crystals are collected by filtration

출처 및 근거

ORD 기록
ord-f1b50b8aa0cb4aacb8adaf96ab0299c9
출처 데이터셋
uspto-grants-1978_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04131611

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