Hydrochloric Acid → 2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine--hydrogen chloride (1/2)
Reaction equation
[CH2:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH2:3][N:2]1C(OCC)=O.[ClH:15]>>[ClH:15].[ClH:15].[CH2:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH2:3][NH:2]1Participants
3
Procedure
10.4 g (51 mmol) of ethyl 2,3-dihydro-1H-pyrrolo-[3,4-c]pyridine-2-carboxylate are refluxed for 15 hours together with 100 ml of concentrated hydrochloric acid. The batch is evaporated, and the crystalline residue is stirred with acetone. The product is filtered off with suction and dried in the air.
Workup
- customThe batch is evaporated
- filtrationThe product is filtered off with suction
- customdried in the air
Sources & evidence
- ORD record
- ord-da275ca293f44d51a9ea56983ed6266b
- Source dataset
- uspto-grants-1994_05
- Patent number
- US05312823
Reaction notes
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