Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408121Generated: October 30, 2026

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

https://huagongshe.com/reaction/408121

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 hydrogenated at 50 PSI of H2 for 8 hours (Parr shaker). The reaction was then concentrated, and the crude oil was dissolved in DCM and poured into saturated Na2CO3 and extracted into DCM. The combined organic fractions were dried, filtered, and concentrated to give tert-butyl octahydro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate (0.99 g, 95% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08758830B2
Source datasetuspto-grants-2014_06
ORD IDord-b500a58117ac40e980df555d490f4c5a
Source noteuspto-grants-2014_06