反応式
[C:1]([OH:6])(=[O:5])[C:2]([CH3:4])=[O:3].[CH2:7](O)[CH2:8][CH2:9][CH3:10]>O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C1(C)C=CC=CC=1>[C:1]([O:6][CH2:7][CH2:8][CH2:9][CH3:10])(=[O:5])[C:2]([CH3:4])=[O:3]参加物
5
反応条件
- 温度
- 25 °C
実験手順
First, a toluene (1 L) solution of pyruvic acid (440 g, 5.0 mol), n-butanol (371 g, 5.0 mol) and p-toluenesulfonic acid monohydrate (2.5 g) was heated and refluxed for 16 hours while removing water under a nitrogen gas stream, whereby a first reaction solution was obtained. Next, the first reaction solution was cooled to room temperature (25° C.). Thereafter, toluene was removed under reduced pressure (40 mmHg) using an evaporator, and the residue was purified by reduced pressure distillation (40 mmHg, 93 to 100° C.), whereby butyl pyruvate (505 g, yield 70%) was obtained.
後処理
- temperaturerefluxed for 16 hours
- customwhile removing water under a nitrogen gas stream, whereby a first reaction solution
- customwas obtained
- customThereafter, toluene was removed under reduced pressure (40 mmHg)
- customan evaporator
- distillationthe residue was purified by reduced pressure distillation (40 mmHg, 93 to 100° C.)
出典と根拠
- ORDレコード
- ord-e3f4b785506842d7aa2cf4bb89d386b6
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08968975B2
関連ノート
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