Hydrochloric Acid → HCID 54694326, compound
Reaction equation
[C:1]1([S:7]Cl)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH:9][C:10]1[CH:15]=[C:14]([CH3:16])[O:13][C:12](=[O:17])[CH:11]=1.Cl>C1C=CC=CC=1>[OH:9][C:10]1[CH:15]=[C:14]([CH3:16])[O:13][C:12](=[O:17])[C:11]=1[S:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Benzenesulfenyl chloride (7.2 g., 0.050 mol) dissolved in benzene (15 ml.) was added to a rapidly stirred slurry of 4-hydroxy-6-methyl-2-pyrone (6.3 g., 0.050 mol) in benzene (135 ml.). There was no apparent reaction at ambient temperature, but upon heating hydrogen chloride was evolved. After heating at reflux for 2 hours, the mixture was cooled and filtered to give 11.6 g. colorless crystals, m. 160°-162.5°C., 99 percent yield.
Workup
- customno apparent reaction at ambient temperature
- temperatureAfter heating
- temperatureat reflux for 2 hours
- temperaturethe mixture was cooled
- filtrationfiltered
- customto give 11.6 g
- custom160°-162.5°C., 99 percent yield
Sources & evidence
- ORD record
- ord-bcf610ae0ec04348811948e49ae4a920
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03931235
Reaction notes
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