Hydrochloric Acid → HCID 178436265, compound
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
Reactant 4
Product 1
Reagents, catalysts & solvents 1
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
- customan exothermic reaction
- temperatureit was heated
- temperatureunder reflux on a steam-bath for 1 hour
- temperatureto cool
- concentrationthe mixture was concentrated under reduced pressure
- customto leave a yellow solid
- stirringthis mixture was stirred at room temperature for 2 hours
- filtrationThe resulting cream solid was filtered off
- washwashed with water
- customdried
- stirringThe solid was stirred with 60-80 petroleum-ether (60 ml) for 2 hours
- filtrationthe resulting white solid was filtered off
- washwashed with 60-80 petroleum-ether
- customdried
Sources & evidence
- ORD record
- ord-a235e78178da4275b01ddca49a6c65d5
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06589724B1
Reaction notes
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