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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373243Generated: October 30, 2026

HCID 131726195, compound → tert-butyl(1S)-1-[3-(2-amino-5-chlorophenoxy)phenyl]ethylcarbamate

https://huagongshe.com/reaction/1373243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131726195HCID 131726195—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
Producttert-butyl(1S)-1-[3-(2-amino-5-chlorophenoxy)phenyl]ethylcarbamateHCID 13172619699.1%

Reaction Steps

5% carbon-palladium (1.1 g) was added to an ethyl acetate (50 ml) solution of tert-butyl(1S)-(-)-1-[3-(5-chloro-2-nitrophenoxy)phenyl]ethylcarbamate (3.5 g, 8.9 mmols). The resulting mixture was hydrogenated at room temperature under atmospheric pressure for 1 hour. The catalyst was removed through filtration, and the filtrate was concentrated under reduced pressure. The residue was purified through silica gel column chromatography to give an oil of tert-butyl(1S)-1-[3-(2-amino-5-chlorophenoxy)phenyl]ethylcarbamate (3.2 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160887B1
Source datasetuspto-grants-2007_01
ORD IDord-71ce2f0581874f33bc43c532f09329aa
Source noteuspto-grants-2007_01