Ammonia → HCID 21392592, compound
Reaction equation
[OH:1][CH:2]([CH3:21])[CH2:3][O:4][C:5]1[C:10]2[C:11](=[O:20])[CH:12]=[C:13]([C:15](OCC)=[O:16])[O:14][C:9]=2[CH:8]=[CH:7][CH:6]=1.[NH3:22]>>[OH:1][CH:2]([CH3:21])[CH2:3][O:4][C:5]1[C:10]2[C:11](=[O:20])[CH:12]=[C:13]([C:15]([NH2:22])=[O:16])[O:14][C:9]=2[CH:8]=[CH:7][CH:6]=1Participants
3
Procedure
By the method of Example 1 (c) 32 parts of 5-(2-hydroxypropoxy)-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester were treated with ethanolic ammonia to give 23.3 parts of 5-(2-hydroxypropoxy)-4-oxo-4H-1-benzopyran-2-carboxamide, which crystallised from a mixture of ethanol and chloroform as a white solid, melting point 229°-231°C.
Sources & evidence
- ORD record
- ord-0c278491ef6d4b7d9e3c3622109d8424
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03933845
Reaction notes
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