Hydrochloric Acid → HCID 13340011, compound
Reaction equation
[NH2:1][CH2:2][C:3]1(O)[C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)[CH2:6][CH2:5][CH2:4]1.[ClH:18]>>[ClH:18].[NH2:1][CH2:2][C:3]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)[CH2:6][CH2:5][CH:4]=1Participants
3
Procedure
10 g. of 1-aminomethyl-6,7-dimethoxy-1-hydroxy-1,2,3,4-tetrahydronaphthalene is treated with HCl as described in Example 3 to yield 1-aminomethyl-6,7-dimethoxy-3,4-dihydronaphthalene HCl; m.p. 197°-199° C.
Sources & evidence
- ORD record
- ord-12c3acc9afed4421a87c7b4298de2825
- Source dataset
- uspto-grants-1984_09
- Patent number
- US04473586
Reaction notes
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