Methanol → HCID 69084602、化合物
反応式
[N:1]1([C:6]2[CH:7]=[C:8]([CH:12]=[CH:13][CH:14]=2)[C:9](O)=[O:10])[CH:5]=[CH:4][N:3]=[N:2]1.B.C1COCC1.CO.O>C1COCC1>[N:1]1([C:6]2[CH:7]=[C:8]([CH2:9][OH:10])[CH:12]=[CH:13][CH:14]=2)[CH:5]=[CH:4][N:3]=[N:2]1参加物
反応条件
- 温度
- 0 °C
実験手順
A cooled (0° C.) solution of the minor isomer 3-(1H-1,2,3-triazol-1-yl)benzoic acid (210 mg; 1.11 mmol) in anh. THF (3 ml) was treated dropwise with a BH3.THF (1.0 M in THF; 2.77 ml; 2.77 mmol), and this mixture was stirred at 0° C., under nitrogen, for 1 h, and then at rt for 17 h. The resulting reaction mixture was then cooled to 0° C., and treated successively with MeOH (10 ml) and water (10 ml). The organic solvents were removed under reduced pressure, and the resulting aq. layer was extracted with DCM (3×10 ml). The mixed organic layers were washed with brine, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by FC (DCM/MeOH=20/1) afforded (3-(1H-1,2,3-triazol-1-yl)phenyl)methanol as a pale yellow solid. LC-MS (conditions A): tR=0.38 min.; [M+H]+: 176.18 g/mol.
後処理
- waitat rt for 17 h
- customThe resulting reaction mixture
- temperaturewas then cooled to 0° C.
- customThe organic solvents were removed under reduced pressure
- extractionthe resulting aq. layer was extracted with DCM (3×10 ml)
- washThe mixed organic layers were washed with brine
- dry with materialdried over anh. MgSO4
- filtrationfiltered
- concentrationconcentrated to dryness under reduced pressure
- customPurification by FC (DCM/MeOH=20/1)
出典と根拠
- ORDレコード
- ord-3bee779f9664457a96ba316bed3c7e23
- 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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