Ethyl Thioglycolate → HCID 54708202, compound

HRID 1112007Notes

Reaction equation

HRID 1112007 reaction equation
[Na].[C:2]([O:6][CH2:7][CH3:8])(=[O:5])[CH2:3][SH:4].[Cl:9][C:10](Cl)=[CH:11][C:12](OCC)=[O:13].CC[O-].[Na+]>C(O)C>[CH2:7]([O:6][C:2]([C:3]1[S:4][C:10]([Cl:9])=[CH:11][C:12]=1[OH:13])=[O:5])[CH3:8]

Participants

6

Procedure

A solution of 23.6 mm of the sodium salt of ethyl thioglycolate in 100 ml of ethanol was added over 5 minutes at 30° C. to a a mixture of 4 g of ethyl dichloroacrylate in 50 ml of ethanol and the mixture was stirred at 25°-30° C. for 15 minutes and was then returned to room temperature. A mixture of 3.22 g of sodium ethylate in 75 ml of ethanol was added thereto and the mixture was stirred for 18 hours. The mixture was concentrated and poured into water and the mixture was extracted with ether. The aqueous phase was acidified with hydrochloric acid and was extracted with ether. The ether phase was evaporated to dryness and the 4.2 g of residue was chromatographed over silica gel. Elution with benzene yielded 1.75 g of 2-ethoxycarbonyl-3-hydroxy-5-chloro-thiophene with Rf = 0.4-0.5.

Workup

  1. customwas then returned to room temperature
  2. additionwas added
  3. stirringthe mixture was stirred for 18 hours
  4. concentrationThe mixture was concentrated
  5. additionpoured into water
  6. extractionthe mixture was extracted with ether
  7. extractionwas extracted with ether
  8. customThe ether phase was evaporated to dryness
  9. customthe 4.2 g of residue was chromatographed over silica gel
  10. washElution with benzene

Sources & evidence

ORD record
ord-3e502f3ebc614bf185bd5e2b05be1a50
Source dataset
uspto-grants-1978_10
Patent number
US04119727

Reaction notes

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