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Water → 4-Methyl-7,7-diphenyl-1,4-oxazepane

HRID 596172
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HRID 596172 반응식
[C:1]([N:6]1[CH2:12][CH2:11][C:10]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[O:9][CH2:8][CH2:7]1)(OCC)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>C(OCC)C>[CH3:1][N:6]1[CH2:12][CH2:11][C:10]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[O:9][CH2:8][CH2:7]1
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참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 20326661HCID 20326661, 화합물HCID 21226445Aluminium lithium hydride

생성물 1

HCID 203266324-Methyl-7,7-diphenyl-1,4-oxazepane

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

7.0 g of 4-carbethoxy-7,7-diphenyl-hexahydro-1,4-oxazepine (Exqmple 3) are added portionwise to the suspension of 0.90 g of lithium aluminum hydride in 80 ml of diethyl ether while stirring and cooling with ice. The mixture is allowed to warm up to room temperature, refluxed for six hours and again cooled to 0° to 5°. Thereupon 0.9 ml of water, 0.9 ml of 15% aqueous sodium hydroxide and 2.7 ml of water are added in this order, the mixture is filtered, the filtrate dried and evaporated. The residue is taken up in acetone and the solution acidified with cyclohexylsulfamic acid in acetone, to yield the 4-methyl-7,7-diphenyl-hexahydro-1,4-oxazepine melting at 199° to 201°.

후처리

  1. temperaturecooling with ice
  2. temperaturerefluxed for six hours
  3. temperatureagain cooled to 0° to 5°
  4. filtrationthe mixture is filtered
  5. customthe filtrate dried
  6. customevaporated

출처 및 근거

ORD 기록
ord-3a87987299144f6890244c531e89608c
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04010166

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