Hydrochloric Acid → HCID 178436265, compound

HRID 1356936Notes

Reaction equation

HRID 1356936 reaction equation
[SH:1][CH2:2][C:3](O)=O.[OH-:6].[K+].[CH:8]([C:10]1[CH:17]=[CH:16][C:13]([CH2:14]Cl)=[CH:12][CH:11]=1)=[CH2:9].Cl>CO>[CH:8]([C:10]1[CH:17]=[CH:16][C:13]([CH2:14][CH2:3][C:2]([OH:6])=[S:1])=[CH:12][CH:11]=1)=[CH2:9]

Participants

6

Procedure

Mercaptoacetic acid (9.2 g, 0.1M) was added over 5 minutes to a stirred solution of potassium hydroxide (12.3 g, 0.22M) in methanol (40 ml). 4-Vinylbenzyl chloride (15.25 g, 0.1M) was then added over 5 minutes during which an exothermic reaction ensued and the mixture turned yellow. The mixture was stirred at room temperature for 5 minutes, then it was heated under reflux on a steam-bath for 1 hour. After being allowed to cool, the mixture was concentrated under reduced pressure to leave a yellow solid. 3M Hydrochloric acid (100 ml) was added to the solid and this mixture was stirred at room temperature for 2 hours. The resulting cream solid was filtered off, washed with water and dried, 20.0 g. The solid was stirred with 60-80 petroleum-ether (60 ml) for 2 hours then the resulting white solid was filtered off, washed with 60-80 petroleum-ether and dried to give 4-vinylbenzylthioacetic acid, 17.8 g (85%). The negative ion mass spectrum was consistent with the structure of the required product as was the 1H nmr spectrum, which also indicated high purity. LCMS showed a single component of the requisite molecular weight.

Workup

  1. customan exothermic reaction
  2. temperatureit was heated
  3. temperatureunder reflux on a steam-bath for 1 hour
  4. temperatureto cool
  5. concentrationthe mixture was concentrated under reduced pressure
  6. customto leave a yellow solid
  7. stirringthis mixture was stirred at room temperature for 2 hours
  8. filtrationThe resulting cream solid was filtered off
  9. washwashed with water
  10. customdried
  11. stirringThe solid was stirred with 60-80 petroleum-ether (60 ml) for 2 hours
  12. filtrationthe resulting white solid was filtered off
  13. washwashed with 60-80 petroleum-ether
  14. customdried

Sources & evidence

ORD record
ord-a235e78178da4275b01ddca49a6c65d5
Source dataset
uspto-grants-2003_07
Patent number
US06589724B1

Reaction notes

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