HRID518779

反应详情

EQUATION

反应方程式

HRID 518779 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

1-(3-Bromophenyl)-3-oxocyclobutanecarbonitrile (2.00 g, 8.00 mmol) was dissolved in DCM (15 mL) and MeOH (15.00 mL), and the mixture was cooled to 0° C. Sodium borohydride (0.333 g, 8.80 mmol) was added to the reaction mixture, and stirring was continued at 0° C. for 1.5 hours. The reaction mixture was quenched with water at 0° C. then warmed to RT. DCM was added, and the mixture was washed with water and brine. The organic layer was dried over sodium sulfate and concentrated under vacuum to afford 2.02 g of 1-(3-bromophenyl)-3-hydroxycyclobutanecarbonitrile (2.02 g, 8.01 mmol, 100% yield) as a pale yellow oil. Mass cal'd: 250.99; MS (ESI pos. ion) m/z: 252.0 [M+H].

WORKUP

后处理

  1. customThe reaction mixture was quenched with water at 0° C.
  2. additionDCM was added
  3. washthe mixture was washed with water and brine
  4. dry with materialThe organic layer was dried over sodium sulfate
  5. concentrationconcentrated under vacuum