반응식
[C:1]1([C:7]2([CH:12]=O)[CH2:11][CH2:10][CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl-].[OH:15][NH3+:16].N1C=CC=CC=1>C(O)C>[C:1]1([C:7]2([CH:12]=[N:16][OH:15])[CH2:11][CH2:10][CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1참가 물질
5
실험 절차
A mixture of the above aldehyde (3.4 g, 20 mmol) and hydroxylammonium chloride (2.9 g, 42 mmol) in a mixture of absolute ethanol (30 ml) and pyridine (3.3 g, 42 mmol) was heated at reflux for 2 h. The solvent was evaporated in vacuo, the residue was treated with absolute ethanol (50 ml) and the suspension filtered. The solvent was evaporated from the filtrate in vacuo and the residue crystallised from a 4/1 mixture of n-heptane and ethyl acetate to give 2.5 g of 1-phenyl-1-cyclopentanecarboxaldehyde oxime.
후처리
- temperaturewas heated
- temperatureat reflux for 2 h
- customThe solvent was evaporated in vacuo
- additionthe residue was treated with absolute ethanol (50 ml)
- filtrationthe suspension filtered
- customThe solvent was evaporated from the filtrate in vacuo
- customthe residue crystallised from a 4/1 mixture of n-heptane and ethyl acetate
출처 및 근거
- ORD 기록
- ord-4915c322d95c4864aebbd6f6a4943ce2
- 출처 데이터셋
- uspto-grants-1997_03
- 특허 번호
- US05608069
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