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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635480Generated: October 30, 2026

Phenethyl bromide → HCID 22618832, compound

https://huagongshe.com/reaction/635480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant1,5-Bis(benzyloxy)pentan-3-oneHCID 22618787—
ReactantHCID 178419670HCID 178419670—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22618832HCID 22618832—

Reaction Steps

To a solution of 1,5-dibenzyloxy-3-pentanone (13.9 g) in tetrahydrofuran (150 ml) was dropwise added a solution of 2-phenylethyl-magnesium bromide, which was prepared from 2-phenylethyl bromide (24 g) and magnesium (3.1 g), in tetrahydrofuran (100 ml) under ice-cooling. The mixture was stirred under ice-cooling for 90 minutes, poured into a saturated aqueous ammonium chloride solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous sodium hydrogencarbonate solution and a saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue obtained was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=4:1) to give the subject compound (8.1 g) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187821B1
Source datasetuspto-grants-2001_02
ORD IDord-b020010bbda0458ab007c5cab772613e
Source noteuspto-grants-2001_02