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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920532Generated: October 31, 2026

Benzylamine → 2-Benzylamino-1-(4-octyloxy-phenyl)ethanol

https://huagongshe.com/reaction/920532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Bromo-1-[4-(octyloxy)phenyl]ethan-1-oneHCID 13435453—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
Product2-Benzylamino-1-(4-octyloxy-phenyl)ethanolHCID 6703246957.6%

Reaction Steps

To a cooled (0° C.) suspension of 2-Bromo-1-(4-octyloxy-phenyl)-ethanone (36.1 g; 110.3 mmol) in EtOH (500 mL) and CHCl3 (100 mL) was added benzylamine (48.2 mL; 441.2 mmol). After 30 minutes the ice-bath was removed and the mixture stirred for another 2 hours at RT. Subsequently the reaction mixture was cooled again to 0° C. and NaBH4 (6.26 g; 165.5 mmol) was added in small portions. The resulting mixture was stirred at 0° C. for 1 hour and thereafter another 4 hours at RT. The reaction mixture was quenched with 1M aqueous HCl (750 mL) at 0° C. and stirred at RT for 1 hour. The reaction mixture was concentrated in vacuo and the residue was partitioned between EtOAc and 2 N aqueous NaOH. The organic layer was dried (Na2SO4), filtered, concentrated in vacuo, and purified by column chromatography (SiO2, EtOAc) to give 2-benzylamino-1-(4-octyloxy-phenyl)-ethanol (22.58 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273017B2
Source datasetuspto-grants-2016_03
ORD IDord-ddf31205701343fabcf7104047482cc0
Source noteuspto-grants-2016_03