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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408201Generated: October 30, 2026

Ethanol → tert-Butyl octahydro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate

https://huagongshe.com/reaction/408201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactanttert-Butyl 1H-pyrrolo[2,3-c]pyridine-1-carboxylateHCID 22646996—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
Producttert-Butyl octahydro-1H-pyrrolo[2,3-c]pyridine-1-carboxylateHCID 5459554095.5%

Reaction Steps

tert-Butyl 1H-pyrrolo[2,3-c]pyridine-1-carboxylate (1.0 g, 4.58 mmol) and PtO2 (0.208 g, 0.916 mmol) were placed in 1:1 EtOH:AcOH (10 mL) and shaken at 50 PSI under H2 for 8 hours. The reaction was then concentrated. The crude oil was dissolved in DCM, poured into saturated Na2CO3 and extracted into DCM. The organic fraction was dried, filtered, and concentrated to give the product as an oil, tert-butyl octahydro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate (0.99 g, 95.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08758830B2
Source datasetuspto-grants-2014_06
ORD IDord-2293eb9397334f139b182a2820fce81d
Source noteuspto-grants-2014_06