HRID1013577

反应详情

EQUATION

反应方程式

HRID 1013577 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

6-Benzenesulfonyl-3,4-dihydro-naphthalene-1-carbonitrile (5.1 g, 17.2 mmol), 70 mL EtOH, and 50 mL acetic acid were placed in a Parr vessel, and 1.0 g of 10% Palladium on carbon (Fluka Chemica Co.) was added. The reaction mixture was shaken for 15 hours under 55 psi hydrogen. The Parr vessel was purged with nitrogen and the reaction mixture was filtered. The filtrate was added to 500 mL water, and the aqueous mixture was extracted twice with 200 mL of EtOAc. The combined organic layers were dried (MgSO4) and evaporated to yield 4.6 g (15.5 mmol, 90%) of 6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalene-1-carbonitrile as an oil. MS: 298 (M+H)+.

WORKUP

后处理

  1. additionwas added
  2. customThe Parr vessel was purged with nitrogen
  3. filtrationthe reaction mixture was filtered
  4. additionThe filtrate was added to 500 mL water
  5. extractionthe aqueous mixture was extracted twice with 200 mL of EtOAc
  6. dry with materialThe combined organic layers were dried (MgSO4)
  7. customevaporated