반응식
[C:1]1([C:7]([C:9]2[CH:10]=[N:11][CH:12]=[CH:13][CH:14]=2)=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[BH4-].[Na+]>CO>[N:11]1[CH:12]=[CH:13][CH:14]=[C:9]([CH:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[OH:8])[CH:10]=1참가 물질
4
실험 절차
50.0 gms of phenyl-3-pyridyl ketone was added to 650 ml of methanol and the system was then cooled to 0° to 5° C. After cooling, 15.5 gms of sodium borohydride was added in 3 parts. After addition, the system was allowed to come to room temperature. The system was then refluxed for 1 hour and stirred for an additional 72 hours at room temperature. The methanol was removed by stripping. Afterwards, 575 ml of 5% HCl solution was added to the residue and the system refluxed for 15 minutes. The acid was neutralized with 50% NaOH solution and the product extracted with methylene chloride to give the 3-pyridylphenylcarbinol as a white solid, m.p. 53° to 60° C.
후처리
- temperaturethe system was then cooled to 0° to 5° C
- temperatureAfter cooling
- additionAfter addition
- customto come to room temperature
- temperatureThe system was then refluxed for 1 hour
- customThe methanol was removed by stripping
- additionAfterwards, 575 ml of 5% HCl solution was added to the residue
- temperaturethe system refluxed for 15 minutes
- extractionthe product extracted with methylene chloride
출처 및 근거
- ORD 기록
- ord-5ec55a0811504211a6dfdbfdd3ca43fb
- 출처 데이터셋
- uspto-grants-1983_10
- 특허 번호
- US04407806
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