Ethanethiol → HCID 20528832, compound

HRID 904076Notes

Reaction equation

HRID 904076 reaction equation
C(S)C.C[O:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][CH:14]([CH2:19][C:20]([OH:22])=[O:21])[CH2:15][C:16]([OH:18])=[O:17])=[CH:8][CH:7]=1>CN(C)C=O>[OH:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][CH:14]([CH2:15][C:16]([OH:18])=[O:17])[CH2:19][C:20]([OH:22])=[O:21])=[CH:8][CH:7]=1

Participants

4

Procedure

To a suspension of 57% sodium hydride-paraffin (2.2 g) in dry dimethylformamide (70 ml) in an atmosphere of nitrogen is slowly added ethanethiol (4.0 ml). The mixture is stirred at room temperature until a clear solution results. To this solution is added a solution of 3-[2-(4-methoxyphenyl)ethyl]-glutaric acid (1.2 g) in dry dimethylformamide (10 ml) and the mixture is heated with stirring in a bath at 165° C. for 6.0 hours. The mixture is then evaporated to dryness in vacuo and the resulting residue is dissolved in water (50 ml), extracted with ether (two 50 ml portions) and the ether extract is discarded. The aqueous solution is acidified with concentrated hydrochloric acid and extracted with ethyl acetate. The ethyl acetate solution is washed with brine, dried with anhydrous magnesium sulfate, and evaporated to a residue. Crystallization of this from chloroform-hexane affords 1.0 g of the title compound, melting point 142°-144° C.

Workup

  1. customresults
  2. temperaturethe mixture is heated
  3. stirringwith stirring in a bath at 165° C. for 6.0 hours
  4. customThe mixture is then evaporated to dryness in vacuo
  5. dissolutionthe resulting residue is dissolved in water (50 ml)
  6. extractionextracted with ether (two 50 ml portions)
  7. extractionthe ether extract
  8. extractionextracted with ethyl acetate
  9. washThe ethyl acetate solution is washed with brine
  10. dry with materialdried with anhydrous magnesium sulfate
  11. customevaporated to a residue
  12. customCrystallization of this from chloroform-hexane

Sources & evidence

ORD record
ord-19309591ce374b9c9e6f6c21f240d80d
Source dataset
uspto-grants-1980_10
Patent number
US04230621

Reaction notes

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