Hydrochloric Acid → HCID 18331747, compound
Reaction equation
C[O:2][C:3]([C:5]1[C:14]2[CH2:13][CH:12]([N:15]3[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]3)[CH2:11][CH2:10][C:9]=2[CH:8]=[CH:7][CH:6]=1)=[O:4].[OH-].[Na+].O.Cl>CO>[N:15]1([CH:12]2[CH2:13][C:14]3[C:5]([C:3]([OH:4])=[O:2])=[CH:6][CH:7]=[CH:8][C:9]=3[CH2:10][CH2:11]2)[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 1.56 g 7-(1-Hexahydroazepinyl)-5,6,7,8-tetrahydronaphthalene-1-carboxylic acid methyl ester, 1.57 mL 12N NaOH, 1.57 mL water in 10 mL methanol was refluxed (70°-80° C.) overnight. TLC showed no starting material remaining. The mixture was neutralized with 6N HCl to pH 5-6 and concentrated to dryness using toluene and methanol. A white solid was recovered and used crude.
Workup
- temperaturewas refluxed (70°-80° C.) overnight
- concentrationconcentrated to dryness
- customA white solid was recovered
Sources & evidence
- ORD record
- ord-7fc56c71bc8c4f5b831616fe38dea90a
- Source dataset
- uspto-grants-1996_08
- Patent number
- US05545755
Reaction notes
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