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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800713Generated: October 28, 2026

Tetrahydrofuran → tert-butyl N-(3-aminophenyl)carbamate

https://huagongshe.com/reaction/1800713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTert-butyl 3-nitrophenylcarbamateHCID 10514065—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Producttert-butyl N-(3-aminophenyl)carbamateHCID 1287722098.4%

Reaction Steps

To a solution of tert-butyl(3-nitrophenyl)carbamate (17.1 g, 71.7 mmol) in ethanol (90 mL)/tetrahydrofuran (30 mL) was added 10% palladium-carbon (1.53 g), and the mixture was stirred at room temperature under a hydrogen atmosphere (3 atm) for 9 hr. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was washed with diethyl ether/hexane mixture to give the title compound (14.7 g, 98%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344135B2
Source datasetuspto-grants-2013_01
ORD IDord-7af70f8f5eae4a5591208561e4bbfe8b
Source noteuspto-grants-2013_01