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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491657Generated: October 31, 2026

Ethyl 1,3,4,5,6,7-hexahydro-5-methyl-2H-pyrrolo[3,4-c]pyridine-2-carboxylate → 5-Methyl-2,3,4,5,6,7-hexahydro-1H-pyrrolo[3,4-c]pyridine

https://huagongshe.com/reaction/1491657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1,3,4,5,6,7-hexahydro-5-methyl-2H-pyrrolo[3,4-c]pyridine-2-carboxylateHCID 18953646—
SolventWaterHCID 962—
Product5-Methyl-2,3,4,5,6,7-hexahydro-1H-pyrrolo[3,4-c]pyridineHCID 15291170—

Reaction Steps

6.3 g (30 mmol) of ethyl 5-methyl-2,3,4,5,6,7-hexahydro-1H-pyrrolo[3, 4-c]pyridine-2-carboxylate and 18.9 g (60 mmol) of Ba(OH)2. 8H2O are refluxed for 15 hours in 75 ml of water. After cooling, the BaCO3 is filtered off with suction, the filtrate is concentrated, and the residue is extracted by boiling five times with 50 ml portions of dioxane. The dioxane solutions are concentrated, and the residue is distilled.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371090
Source datasetuspto-grants-1994_12
ORD IDord-8726b60098e44e72a250abbcf842d3f0
Source noteuspto-grants-1994_12