반응식
[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]참가 물질
5
반응 조건
- 온도
- 25 °C
실험 절차
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.
후처리
- 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.)
출처 및 근거
- ORD 기록
- ord-e3f4b785506842d7aa2cf4bb89d386b6
- 출처 데이터셋
- uspto-grants-2015_03
- 특허 번호
- US08968975B2
연결된 노트
불러오는 중…