Pyridine → N-benzoyl-4-hydroxypiperidine
反応式
[C:1](Cl)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH:10][CH:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1.N1C=CC=CC=1>ClCCl>[C:1]([N:14]1[CH2:15][CH2:16][CH:11]([OH:10])[CH2:12][CH2:13]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
5
実験手順
A solution of 73.1 g (520 mmol) of benzoyl chloride in 70 ml of dichloromethane was added dropwise to a solution of 50.0 g (495 mmol) of 4-hydroxypiperidine and 260 ml of pyridine in 260 ml of dichloromethane at 0° to 15° C. The mixture was stirred at room temperature for 3 h and white crystals (pyridine hydrochloride) thus precipitated were filtered out. The filtrate was concentrated and a remaining oil was purified by silica gel column chromatography (CHCl3 :CH3OH=95:5) to give 79.8 g (yield: 79%) of the intended compound:
後処理
- customwhite crystals (pyridine hydrochloride) thus precipitated
- filtrationwere filtered out
- concentrationThe filtrate was concentrated
- customa remaining oil was purified by silica gel column chromatography (CHCl3 :CH3OH=95:5)
出典と根拠
- ORDレコード
- ord-12537e93d9504a13a53cebdd680e5324
- 出典データセット
- uspto-grants-1990_12
- 特許番号
- US04977165
反応ノート
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