Carbon tetrabromide → 4-(Bromomethyl)-2-(difluoromethoxy)pyridine
反応式
[F:1][CH:2]([F:12])[O:3][C:4]1[CH:9]=[C:8]([CH2:10]O)[CH:7]=[CH:6][N:5]=1.C(Br)(Br)(Br)[Br:14].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>C(Cl)Cl>[Br:14][CH2:10][C:8]1[CH:7]=[CH:6][N:5]=[C:4]([O:3][CH:2]([F:12])[F:1])[CH:9]=1参加物
5
実験手順
A solution of (2-(difluoromethoxy)pyridin-4-yl)methanol (250 mg; 1.42 mmol) in anh. DCM (12 ml) was treated at rt with CBr4 (473 mg; 1.42 mmol), and with PPh3 (374 mg; 1.42 mmol). The resulting mixture was further stirred at rt, under nitrogen, for 1 h. Concentration to dryness under reduced pressure, and subsequent purification by FC (DCM) afforded 4-(bromomethyl)-2-(difluoromethoxy)pyridine as a yellow oil which was directly used for the next reaction. LC-MS (conditions A): tR=0.78 min.
後処理
- concentrationConcentration to dryness
- customunder reduced pressure, and subsequent purification by FC (DCM)
出典と根拠
- ORDレコード
- ord-9fa2bb710cb1473db596aa723f0f6f8d
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09242970B2
反応ノート
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