반응식
[OH:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[C:4]([O:10][CH3:11])[C:3]=1[C:12](=[O:14])[CH3:13].[C:15](=[S:17])=S.O.S(=O)(=O)(O)O>C1(C)C=CC=CC=1>[OH:14][C:12]1[C:3]2[C:2](=[CH:7][C:6]([O:8][CH3:9])=[CH:5][C:4]=2[O:10][CH3:11])[O:1][C:15](=[S:17])[CH:13]=1참가 물질
실험 절차
336.0 g of potassium t-butoxy was suspended in 2 liters of toluene. Under cooling on ice, 2 liters of 196.0 g of 2'-hyroxy-4',6'-dimethoxyacetophenone and 72.0 ml carbon disulfide in toluene were added dropwise to said suspension. The mixture was stirred for 20 hours at room temperature, and 7 liters of water was added for extraction of a toluene layer. This toluene solution was adjusted to pH 4-5 by addition of 800 ml of 10% sulfuric acid (aq.) and was then stirred for 5 hours at room temperature. The solution was allowed to stand overnight. The resulting yellow crystals were collected by filtration under reduced pressure, sufficiently washed with water and dried at 50° C. for 3 days under reduced pressure, thus giving rise to 160.0 g crude 4-hydroxy-5,7-dimethoxychromene-2-thion.
후처리
- additionwere added dropwise
- stirringwas then stirred for 5 hours at room temperature
- waitto stand overnight
- filtrationThe resulting yellow crystals were collected by filtration under reduced pressure
- washsufficiently washed with water
- customdried at 50° C. for 3 days under reduced pressure
출처 및 근거
- ORD 기록
- ord-387f65fb15364149b6a36464951de885
- 출처 데이터셋
- uspto-grants-1996_05
- 특허 번호
- US05521216
연결된 노트
불러오는 중…