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HRID 2196263作成日:2026年10月24日

Hydrochloric Acid → (S)-2-(5-Bromo-2-fluoro-phenyl)-2-methyl-oxirane

https://huagongshe.com/ja/reaction/2196263

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Ethanol hexaneHCID 21879635—
反応物(S)-2-(5-Bromo-2-fluoro-phenyl)-propane-1,2-diolHCID 66665442—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物(S)-2-(5-Bromo-2-fluoro-phenyl)-2-methyl-oxiraneHCID 86650263—

反応条件

温度2.5 °C

反応手順

To a solution of (S)-2-(5-bromo-2-fluoro-phenyl)-propane-1,2-diol (37.35 g, 150 mmol) in CH2Cl2 (400 ml) was added under argon NEt3 (41.8 ml, 300 mmol) and dropwise mesyl chloride (12.8 ml, 165 mmol) at 0-5° C. After stirring for 0.5 h at 0-5° C. the reaction mixture was added to cold 1N HCl and extracted with CH2Cl2. Combined extracts were washed with 1N HCl, H2O and saturated NaHCO3 solution, dried over MgSO4, filtered and concentrated. The crude mesylate was dissolved in TBME (500 ml) and 200 ml 2N aqueous NaOH and after stirring for 2 h at 25° C. the mixture was extracted with TBME. Combined extracts were washed with NaH2PO4 solution and brine, dried over MgSO4, filtered and concentrated to provide the (S)-enantiomer as a colorless oil: 78% ee (Chiralpak AS-H 1218, hexane-EtOH 97:3, 0.4 mL/min); TLC (hexane-EtOAc 3:1): Rf=0.69; HPLC RtH5=1.186 min; 1H NMR (360 MHz, CDCl3): δ 7.46 (dd, 1H), 7.30 (m, 1H), 6.83 (dd, 1H), 2.88 (d, 1H), 2.72 (d, 1H), 1.59 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08338413B1
出典データセットuspto-grants-2012_12
ORD IDord-787b067baa8142d0a6780bc07dea7b8e
出典メモuspto-grants-2012_12