Dimethyl Sulfoxide → HCID 70391478, compound

HRID 1381690Notes

Reaction equation

HRID 1381690 reaction equation
[C:1]([CH:5]1[CH2:9]SC[C:6]1=O)([O:3][CH3:4])=[O:2].C[O-].[Na+].CI.[CH3:16][S:17]([CH3:19])=[O:18]>O>[C:1]([C:5]1([CH3:9])[CH2:19][S:17](=[O:18])[CH2:16][CH2:6]1)([O:3][CH3:4])=[O:2]

Participants

6

Procedure

To a solution of 4.65 g (29.0 mmol) of 4-carbomethoxytetrahydro-3-thiophenone in 20 ml of dry DMSO cooled in a cold-water bath at 12° C. under argon was added 1.73 g (32.0 mmol) of sodium methoxide. The mixture was stirred 30 minutes and a solution of 4.97 g (35.0 mmol) of methyl iodide in 1 ml of dry DMSO was added dropwise. The mixture was stirred overnight at room temperature, than diluted with water (60 ml) and extracted with methylene chloride (3×75 ml). The extract was washed with water (50 ml) and brine, dried over sodium sulfate, filtered, and concentrated in vacuo to give 5.4 g of an oil. The oil was flash chromatographed on silica gel eluting with 3:1 hexane:ether to give 1.49 g (30%) of the product as an oil; NMR (deuteriochloroform): δ 3.76 (S, 3H), 3.70 (m, 1H), 3.50 (dd, 1H), 3.30 (dd, 1H), 2.83 (d, 1H), 1.46 (S, 3H).

Workup

  1. stirringThe mixture was stirred overnight at room temperature
  2. extractionextracted with methylene chloride (3×75 ml)
  3. washThe extract was washed with water (50 ml) and brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-de5d7b2c8bf14f43b4c6ec3553f9052d
Source dataset
uspto-grants-1989_02
Patent number
US04803286

Reaction notes

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