Ammonia → 2,3-Dihydro-3,3-dimethylbenzofuran-5-carboxylic acid amide
Reaction equation
[CH3:1][C:2]1([CH3:14])[C:6]2[CH:7]=[C:8]([C:11](Cl)=[O:12])[CH:9]=[CH:10][C:5]=2[O:4][CH2:3]1.[NH3:15]>>[CH3:1][C:2]1([CH3:14])[C:6]2[CH:7]=[C:8]([C:11]([NH2:15])=[O:12])[CH:9]=[CH:10][C:5]=2[O:4][CH2:3]1Participants
3
Procedure
The product of stage (b) (4.2 g) was added dropwise to excess aqueous ammonia with stirring and ice cooling. After 1 hour the white precipitate was filtered off and recrystallised from ethanol to give 1.1 g of title product, mp 136°-138° C.
Workup
- filtrationAfter 1 hour the white precipitate was filtered off
- customrecrystallised from ethanol
Sources & evidence
- ORD record
- ord-1bf2508ee087481386050f91d455139e
- Source dataset
- uspto-grants-1982_06
- Patent number
- US04333759
Reaction notes
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