Ethanol → 1-(Mercaptomethyl)cyclopropaneacetic acid ethyl ester

HRID 1986033Notes

Reaction equation

HRID 1986033 reaction equation
[SH:1][CH2:2][C:3]1([CH2:6][C:7]([OH:9])=[O:8])[CH2:5][CH2:4]1.S(=O)(=O)(O)O.[CH2:15](O)[CH3:16]>>[CH2:15]([O:8][C:7](=[O:9])[CH2:6][C:3]1([CH2:2][SH:1])[CH2:5][CH2:4]1)[CH3:16]

Participants

4

Conditions

Temperature
20.5 °C

Procedure

To a 3 L flask, a solution of 1-(mercaptomethyl)cyclopropaneacetic acid (204.5 g) in ethanol (1000 ml) was charged. 96% sulfuric acid (22.73 g) was added, and the reaction mixture was stirred for 3 h at 19-22° C. The reaction mixture was concentrated to ¼ of its volume at 50° C. under reduced pressure, and the residue was partitioned between water (1000 ml) and ethyl acetate (200 ml). The organic phase was separated, washed with 10% NaHCO3 (400 ml), and dried for 2 h over anhydrous sodium sulfate. The mixture was filtered and evaporated at 50° C., under reduced pressure, to afford 197.9 g of the crude 1-(mercaptomethyl)cyclopropaneacetic acid ethyl ester, as a slightly colored liquid with a strong, unpleasant odor.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. customto ¼ of its volume at 50° C. under reduced pressure
  3. customthe residue was partitioned between water (1000 ml) and ethyl acetate (200 ml)
  4. customThe organic phase was separated
  5. washwashed with 10% NaHCO3 (400 ml)
  6. dry with materialdried for 2 h over anhydrous sodium sulfate
  7. filtrationThe mixture was filtered
  8. customevaporated at 50° C., under reduced pressure

Sources & evidence

ORD record
ord-17f05e5df63d4dc1bf912b8d95e4b9ce
Source dataset
uspto-grants-2009_06
Patent number
US07547787B2

Reaction notes

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