Hydrochloric Acid → HCID 10997132, compound
Reaction equation
C[O:2][C:3]([C@@H:5]1[C@H:9]([CH3:10])[CH2:8][C:7](=[O:11])[CH2:6]1)=[O:4].Cl>>[C:3]([C@@H:5]1[C@H:9]([CH3:10])[CH2:8][C:7](=[O:11])[CH2:6]1)([OH:4])=[O:2]Participants
3
Procedure
1.18 g of (3S, 4R)-3-methoxycarbonyl-4-methylcyclopentanone was added to 20 ml of 3N-hydrochloric acid, and the mixture was refluxed for 2 hours. The resultant mixture was cooled down to room temperature, and concentrated to dryness. The residue was purified by distillation under a reduced pressure, and thus 0.858 g of the titled compound was obtained.
Workup
- temperaturethe mixture was refluxed for 2 hours
- concentrationconcentrated to dryness
- distillationThe residue was purified by distillation under a reduced pressure
Sources & evidence
- ORD record
- ord-985eaa37d2ae4d1da45eeea1e0b31458
- Source dataset
- uspto-grants-1994_07
- Patent number
- US05329042
Reaction notes
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