Dimethyl Sulfoxide → 2-Oxoethyl butyrate

HRID 1369177Notes

Reaction equation

HRID 1369177 reaction equation
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[C:15]([O:20][CH2:21][CH2:22][OH:23])(=[O:19])[CH2:16][CH2:17][CH3:18].CS(C)=O.CCN(CC)CC>C(Cl)Cl>[C:15]([O:20][CH2:21][CH:22]=[O:23])(=[O:19])[CH2:16][CH2:17][CH3:18]

Participants

6

Conditions

Temperature
0 °C

Procedure

To a mechanically stirred suspension of P2O5 (42.53 g, 150 mmol) in dry DCM (100 ml) at 0° C., was slowly added 30 (11.0 g, 83 mmol), followed by DMSO (13 g, 11.8 ml, 166 mmol). After stirring at 0° C. for 1 h, the ice bath was removed and the mixture further stirred at rt for 1.5 h. It was then cooled to 0° C., and then Et3N (42 g, 58 ml, 416 mmol) was slowly added. The reaction was then left with stirring for 6 hours at room temperature. The reaction was quenched by adding 1.0 M HCl (60 ml) at 0° C., and left with stirring for 30 minutes at 0° C. The organic layer was then washed with water (2×250 ml), dried, filtered and evaporated to afford 24 (6.60 g, 51 mmol, 61%) as a yellow liquid, that was used in the next step without any further purification.

Workup

  1. customthe ice bath was removed
  2. stirringthe mixture further stirred at rt for 1.5 h
  3. temperatureIt was then cooled to 0° C.
  4. waitThe reaction was then left
  5. stirringwith stirring for 6 hours at room temperature
  6. customThe reaction was quenched
  7. additionby adding 1.0 M HCl (60 ml) at 0° C.
  8. waitleft
  9. stirringwith stirring for 30 minutes at 0° C
  10. washThe organic layer was then washed with water (2×250 ml)
  11. customdried
  12. filtrationfiltered
  13. customevaporated

Sources & evidence

ORD record
ord-0c9830ed7aa7493da7654f243898bb11
Source dataset
uspto-grants-2003_06
Patent number
US06576776B1

Reaction notes

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