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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106848Generated: October 31, 2026

Ethyl 4-[2-benzyloxy-5-bromophenylacetamido]benzoate → ethyl 4-[N-(2-benzyloxy-5-bromophenethyl)amino]benzoate

https://huagongshe.com/reaction/1106848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-[2-benzyloxy-5-bromophenylacetamido]benzoateHCID 54475189—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Productethyl 4-[N-(2-benzyloxy-5-bromophenethyl)amino]benzoateHCID 2267552157.7%

Reaction Steps

A mixture of ethyl 4-[2-benzyloxy-5-bromophenylacetamido]-benzoate (2.5 g) and BH3. THF (10 mM) in THF (60 ml) was stirred at 50° C. for 2 hours, cooled (ice bath) and diluted with 2N HCl solution (10 ml) and diethyl ether (50 ml). The organic layer was separated, dried (MgSO4) and evaporated. The residue was purified by chromatography on silica gel eluting with dichloromethane to give ethyl 4-[N-(2-benzyloxy-5-bromophenethyl)amino]benzoate (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057345
Source datasetuspto-grants-2000_05
ORD IDord-d10f7b685c424e7cbc4cc8424bbb1e1c
Source noteuspto-grants-2000_05