Sodium Hydroxide → HCID 21522824, compound
Reaction equation
C([O:3][C:4](=[O:22])[CH2:5][C:6]1([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[O:10][C:9]2[CH:11]=[CH:12][C:13]([Cl:15])=[CH:14][C:8]=2[O:7]1)C.[OH-].[Na+]>C(O)C>[C:16]1([C:6]2([CH2:5][C:4]([OH:22])=[O:3])[O:10][C:9]3[CH:11]=[CH:12][C:13]([Cl:15])=[CH:14][C:8]=3[O:7]2)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 32 g. of ethyl(2-phenyl-5-chloro-1,3-benzodioxol-2-yl)acetate, 200 cc. of 95% ethanol and 150 cc. of 4% NaOH is refluxed for 2 hours. The alcohol is then removed under vacuum and, after cooling, the mixture is acidified with dilute HCl. The precipitated solid is filtered off and recrystallised from benzene-hexane, m.p. 117°-119°C.
Workup
- additionA mixture of 32 g
- customThe alcohol is then removed under vacuum
- temperatureafter cooling
- filtrationThe precipitated solid is filtered off
- customrecrystallised from benzene-hexane, m.p. 117°-119°C.
Sources & evidence
- ORD record
- ord-ef664a4dbe6d45ef90d8cd0c3a64abbc
- Source dataset
- uspto-grants-1976_07
- Patent number
- US03969368
Reaction notes
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