Potassium ethanethioate → (S)-2-(Acetylthio)-4,4-dimethylpentanoic acid

HRID 1720984Notes

Reaction equation

HRID 1720984 reaction equation
[C:1]([O-:4])(=[S:3])[CH3:2].[K+].Br[C@H:7]([CH2:11][C:12]([CH3:15])([CH3:14])[CH3:13])[C:8]([OH:10])=[O:9]>C(#N)C>[C:1]([S:3][C@@H:7]([CH2:11][C:12]([CH3:15])([CH3:14])[CH3:13])[C:8]([OH:10])=[O:9])(=[O:4])[CH3:2]

Participants

4

Procedure

A slurry of potassium thioacetate (750 mg, 6.58 mmol) and acetonitrile (10 ml, molecular sieves dried) was cooled to 0° C. and treated with a solution of (R)-2-bromo-4,4-dimethylpentanoic acid from part (a) in acetonitrile (2 ml) over 5 minutes. The reaction mixture was allowed to warm to room temperature and stirred for 2.5 hours. The slurry was filtered. The filtrate was concentrated in vacuo. The residue was diluted in ether (50 ml), washed with two portions of 5% aqueous sodium thiosulfate (50 ml) and brine (25 ml), dried (magnesium sulfate)0 and concentrated in vacuo. The pale yellow oil was purified by flash chromatography (Merck silica gel, 12×3 cm., 10% methanol/methylene chloride) affording 575 mg of title product as a pale yellow oil.

Workup

  1. filtrationThe slurry was filtered
  2. concentrationThe filtrate was concentrated in vacuo
  3. additionThe residue was diluted in ether (50 ml)
  4. washwashed with two portions of 5% aqueous sodium thiosulfate (50 ml) and brine (25 ml), dried (magnesium sulfate)0
  5. concentrationconcentrated in vacuo
  6. customThe pale yellow oil was purified by flash chromatography (Merck silica gel, 12×3 cm., 10% methanol/methylene chloride)

Sources & evidence

ORD record
ord-e54c67dfa7254bb3a112f234e7a67127
Source dataset
uspto-grants-1996_04
Patent number
US05508272

Reaction notes

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