Thionyl Chloride → 3-(3-(4-(Trifluoromethoxy)phenoxy)azetidin-1-yl)propionyl chloride
反応式
[F:1][C:2]([F:21])([F:20])[O:3][C:4]1[CH:19]=[CH:18][C:7]([O:8][CH:9]2[CH2:12][N:11]([CH2:13][CH2:14][C:15](O)=[O:16])[CH2:10]2)=[CH:6][CH:5]=1.S(Cl)([Cl:24])=O>>[F:1][C:2]([F:21])([F:20])[O:3][C:4]1[CH:19]=[CH:18][C:7]([O:8][CH:9]2[CH2:12][N:11]([CH2:13][CH2:14][C:15]([Cl:24])=[O:16])[CH2:10]2)=[CH:6][CH:5]=1参加物
3
実験手順
3-(3-(4-(trifluoromethoxy)phenoxy)azetidin-1-yl)propionic acid (400 mg, 1.31 mmol) was dissolved in thionyl chloride, raised the temperature to reflux for 3 h, spun dry, residuals were washed by an appropriate amount of ethyl ether, generated 423 mg target product, yield was 100%, directly put to the next reaction step.
後処理
- temperatureraised the temperature
- temperatureto reflux for 3 h
- customspun dry
- washresiduals were washed by an appropriate amount of ethyl ether
- customdirectly put to the next reaction step
出典と根拠
- ORDレコード
- ord-9042d2087b6749eca426f18487e69e36
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08563547B2
反応ノート
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