Sodium Cyanide → (3R)-3-Hydroxy-4,4-dimethylpentanenitrile

HRID 515183Notes

Reaction equation

HRID 515183 reaction equation
[OH:1][C@@H:2]([C:15]([CH3:18])([CH3:17])[CH3:16])[CH2:3]OS(C1C=CC(C)=CC=1)(=O)=O.[C-:19]#[N:20].[Na+]>CS(C)=O>[OH:1][C@@H:2]([C:15]([CH3:16])([CH3:17])[CH3:18])[CH2:3][C:19]#[N:20]

Participants

4

Conditions

Temperature
60 °C

Procedure

To a stirred solution of 4-methyl-benzenesulfonic acid [(2S)-2-hydroxy-3,3-dimethyl-butyl]ester (4.2 g, 14.4 mmol) in dimethylsulfoxide (30 ml) is added sodium cyanide (3.6 g, 71.9 mmol) and the reaction mixture is heated at 60° C. for 16 h. The reaction mixture is poured onto water (100 ml) and extracted with ethyl acetate (3×30 ml). The combined organic layers are washed with water (3×50 ml), dried over sodium sulfate and evaporated to dryness affording (3R)-3-hydroxy-4,4-dimethyl-pentanenitrile, which is used in next step without further purification (1.3 g, 10.2 mmol, 71%).

Workup

  1. additionThe reaction mixture is poured onto water (100 ml)
  2. extractionextracted with ethyl acetate (3×30 ml)
  3. washThe combined organic layers are washed with water (3×50 ml)
  4. dry with materialdried over sodium sulfate
  5. customevaporated to dryness

Sources & evidence

ORD record
ord-f5f3d00ccbd0431e9e5eccd9d5fc02e8
Source dataset
uspto-grants-2015_08
Patent number
US09108936B2

Reaction notes

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