Hydrochloric Acid → HCID 13669829, compound
Reaction equation
[Cl:1][C:2]1[C:15]2[O:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:16])[C:6]=2[CH:5]=[CH:4][C:3]=1[O:17][CH2:18][C:19]([O:21]CC)=[O:20].[OH-].[Na+].Cl>O>[Cl:1][C:2]1[C:15]2[O:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:16])[C:6]=2[CH:5]=[CH:4][C:3]=1[O:17][CH2:18][C:19]([OH:21])=[O:20]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of this ester (0.9 g), sodium hydroxide (0.7 g) and water (40 ml) was refluxed for 1 hour. After cooling, the mixture was rendered acidic with hydrochloric acid and the solid crystal was recovered by filtration, washed with water and dried. Recrystallization from ethanol gave 0.7 g of 4-chloro-9-oxo-9H-xanthene-3-yloxyacetic acid. m.p. 280°-281° C.
Workup
- temperaturewas refluxed for 1 hour
- temperatureAfter cooling
- filtrationthe solid crystal was recovered by filtration
- washwashed with water
- customdried
- customRecrystallization from ethanol
Sources & evidence
- ORD record
- ord-a1a33d4456b54d71b53443487db8fa89
- Source dataset
- uspto-grants-1989_03
- Patent number
- US04816479
Reaction notes
Loading…