Hydrochloric Acid → HCID 12906310, compound
Reaction equation
C(O[C:6]([N:8]([N:10]1[CH2:18][C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:11]1)C)=O)(C)(C)C.[ClH:19]>>[ClH:19].[CH3:6][NH:8][N:10]1[CH2:18][C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:11]1Participants
3
Procedure
To the crude N-(t-butyloxycarbonyl-N-methylamino)dihydroisoindole from the above preparation was added 25 ml of concentrated hydrochloric acid. The reaction mixture was allowed to stir for one hour. Evaporation of the mixture to dryness and recrystallization of the residue from ethanolether gave 5.6 g of the desired product as a gummy solid, mp: 79°-89°. The IR and NMR were consistent with the proposed structure.
Workup
- customEvaporation of the mixture
- customto dryness and recrystallization of the residue from ethanolether
Sources & evidence
- ORD record
- ord-de7a3c82ec4a42599a0984958372f6a1
- Source dataset
- uspto-grants-1982_03
- Patent number
- US04321200
Reaction notes
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