Hydrochloric Acid → HCID 20304582, compound
Reaction equation
N[C:2]1[C:15]2[C:14](=[O:16])[CH:13]=[C:12]([C:17]([O:19]CC)=[O:18])[O:11][C:10]=2[C:9]([CH2:22][CH2:23][CH3:24])=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][CH2:7]2.N([O-])=O.[Na+].[ClH:29]>O>[Cl:29][C:2]1[C:15]2[C:14](=[O:16])[CH:13]=[C:12]([C:17]([OH:19])=[O:18])[O:11][C:10]=2[C:9]([CH2:22][CH2:23][CH3:24])=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][CH2:7]2Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 5amino-6,7,8,9-tetrahydro-4-oxo-10-propyl-4H-naphtho[2,3-b]pyran-2-carboxylate (7.2 g) in concentrated hydrochloric acid (90 ml) was treated with sodium nitrite (1.8 g) in water (15 ml) with stirring at 0° over 15 minutes.
Sources & evidence
- ORD record
- ord-0d9666372f3644cfbd7be4982aedbcaa
- Source dataset
- uspto-grants-1979_06
- Patent number
- US04159273
Reaction notes
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