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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373220Generated: November 2, 2026

Tert-butyl[3-(5-benzyloxy-2-nitrophenoxy)benzyl]carbamate → Tert-butyl[3-(2-amino-5-hydroxyphenoxy)benzyl]carbamate

https://huagongshe.com/reaction/1373220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl[3-(5-benzyloxy-2-nitrophenoxy)benzyl]carbamateHCID 21073109—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl[3-(2-amino-5-hydroxyphenoxy)benzyl]carbamateHCID 2107310798.8%

Reaction Steps

5% carbon-palladium (3.2 g) was added to an ethyl acetate (300 ml) solution of tert-butyl[3-(5-benzyloxy-2-nitrophenoxy)benzyl]carbamate (10.5 g, 23.3 mmols). The resulting mixture was hydrogenated at room temperature under atmospheric pressure. The catalyst was removed through filtration, and the filtrate was concentrated under reduced pressure to give a brown oil of tert-butyl[3-(2-amino-5-hydroxyphenoxy)benzyl]carbamate (7.6 g, 98.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160887B1
Source datasetuspto-grants-2007_01
ORD IDord-8594ec69f87943be9b2f8a795fea13fc
Source noteuspto-grants-2007_01