Pyridine → Carbonic acid 1-chloroethyl ester (1S,2S)-2-fluorocyclohexyl ester
反応式
Cl[C:2]([O:4][CH:5]([Cl:7])[CH3:6])=[O:3].N1C=CC=CC=1.[F:14][C@H:15]1[CH2:20][CH2:19][CH2:18][CH2:17][C@@H:16]1[OH:21].CC1(C)C2(CS(O)(=O)=O)C(CC1CC2)=O>ClCCl>[F:14][C@H:15]1[CH2:20][CH2:19][CH2:18][CH2:17][C@@H:16]1[O:21][C:2](=[O:3])[O:4][CH:5]([Cl:7])[CH3:6]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a mixture of 1-chloroethyl chloroformate (1.0 mL), pyridine (1.0 mL), and dichloromethane (30 mL), (1S,2S)-2-fluorocyclohexanol [CSA No. 292150-03-9] (900 mg) dissolved in dichloromethane (10 mL) was added at −78° C. After stirring the resulting mixture overnight at room temperature, dichloromethane (30 mL) was added to the mixture. The resulting mixture was sequentially washed with 0.5 N hydrochloric acid and saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The resulting mixture was filtered, and the filtrate obtained was concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography (mixed solvent of heptane-ethyl acetate) to obtain the captioned compound (480 mg).
後処理
- additionwas added at −78° C
- washThe resulting mixture was sequentially washed with 0.5 N hydrochloric acid and saturated aqueous sodium chloride solution
- dry with materialdried over anhydrous magnesium sulfate
- filtrationThe resulting mixture was filtered
- customthe filtrate obtained
- concentrationwas concentrated under reduced pressure
- customThe residue obtained
- customwas purified by silica gel column chromatography (mixed solvent of heptane-ethyl acetate)
出典と根拠
- ORDレコード
- ord-8aca998ab7894999ad3148bfa6ff2ca9
- 出典データセット
- uspto-grants-2013_05
- 特許番号
- US08436009B2
反応ノート
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