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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355754Generated: October 26, 2026

Acetic Acid → ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate

https://huagongshe.com/reaction/355754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl 4-(aminomethyl)benzoateHCID 436161—
Reactant2-(Benzyloxy)-5-bromobenzaldehydeHCID 733087—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Productethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoateHCID 22675503—

Reaction Steps

2-Benzyloxy-5-bromobenzaldehyde and ethyl 4-aminomethylbenzoate were heated together at 100° C. for 1 hour. The mixture was cooled, dissolved in ethanol (100 ml) and sodium borohydride (1.3 g) was added. The mixture was stirred for 18 hours at ambient temperature, acidified with acetic acid and water (200 ml) was added. The mixture was extracted with diethyl ether (4×100 ml), the extracts washed with saturated aqueous NaHCO3, dried (MgSO4), filtered and evaporated to give ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate which was purified by chromatography on silica gel eluting with CH2Cl2 then 5% ethyl acetate/CH2Cl2 (yield 11.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834468
Source datasetuspto-grants-1998_11
ORD IDord-ac2592b1d7e9403f99739f686d9d8a9c
Source noteuspto-grants-1998_11