Anthranilic Acid → HCID 12701622, compound
Reaction equation
[CH3:1][C:2]1[CH:10]=[C:6]([C:7]([OH:9])=[O:8])[C:5]([NH2:11])=[CH:4][CH:3]=1.[C:12]([OH:21])(=[O:20])[C:13]1C(=CC=[CH:18][CH:19]=1)N>>[C:7]([C:6]1[CH:10]=[C:2]([CH3:1])[CH:3]=[CH:4][C:5]=1[NH:11][CH:13]1[CH2:19][CH2:18][O:21][C:12]1=[O:20])([OH:9])=[O:8]Participants
3
Procedure
In the method of the Reference Example 1, 5-methylanthranilic acid was reacted in the place of anthranilic acid to obtain α[(2-carboxy-4-methylphenyl)amino]-γ-butyrolactone, melting point: 199°-200° C.
Sources & evidence
- ORD record
- ord-d9b725b13d83467f828c3caf7a5b719c
- Source dataset
- uspto-grants-1979_05
- Patent number
- US04154731
Reaction notes
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