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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988267Generated: November 4, 2026

2-(3-t-Butyl-4-hydroxyphenyl)-1-(1,3,4-oxadiazol-2-yl)ethylcarbamic acid benzyl ester → 2-(3-t-Butyl-4-hydroxyphenyl)-1-(1,3,4-oxadiazol-2-yl)ethylamine

https://huagongshe.com/reaction/1988267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-t-Butyl-4-hydroxyphenyl)-1-(1,3,4-oxadiazol-2-yl)ethylcarbamic acid benzyl esterHCID 86760900—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product2-(3-t-Butyl-4-hydroxyphenyl)-1-(1,3,4-oxadiazol-2-yl)ethylamineHCID 1781921197%

Reaction Steps

To a solution of 2-(3-t-butyl-4-hydroxyphenyl)-1-(1,3,4-oxadiazol-2-yl)ethylcarbamic acid benzyl ester (1.25 g, 3.16 mmol) in methanol (30 ml), 10% palladium carbon (130 mg) was added and stirred in a hydrogen atmosphere at room temperature for 1 day. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure; the thus obtained residue was subjected to silica gel column chromatography (developing solvent: chloroform:methanol:aqueous ammonia=100:10:1), giving the titled compound (0.80 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553969B1
Source datasetuspto-grants-2009_06
ORD IDord-9b220cad92d14557a09cd4eac5ff3a19
Source noteuspto-grants-2009_06