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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333324Generated: October 29, 2026

Benzyl Bromide → HCID 68746130, compound

https://huagongshe.com/reaction/333324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-[(4-Bromophenyl)methyl]-3-[(tert-butoxycarbonyl)amino]propanoic acidHCID 44891005—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68746130HCID 687461307.1%

Reaction Steps

A suspension of 3-(4-bromo-phenyl)-2-(tert-butoxycarbonylamino-methyl)-propionic acid (496 mg, 1.385 mmol), K2CO3 (383 mg, 2.77 mmol) and BnBr (0.493 ml, 4.15 mmol) in DMF (3 ml) was allowed to stir under nitrogen for 60 hours. The reaction mixture was cooled, and brine was added. The product was extracted with EtOAc, washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel (eluent: heptane/EtOAc=100:0 to 50:50) and then purified by RP-HPLC (XBridge Prep Phenyl OBD, H2O (0.1% NH4OH)/CH3CN) to give benzyl 2-(4-bromobenzyl)-3-(tert-butoxycarbonylamino)propanoate (44 mg); Retention time=1.67 minutes (condition B); MS (ES+)=348.0 (m-Boc+2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877815B2
Source datasetuspto-grants-2014_11
ORD IDord-961a8c8010f9448a8efc1f7f2f70ed13
Source noteuspto-grants-2014_11