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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131765Generated: October 25, 2026

Sodium Iodide → Methyl 3-(2-(benzyloxy)-5-bromophenyl)-3-phenylpropanoate

https://huagongshe.com/reaction/131765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromo-3,4-dihydro-4-phenyl-2H-1-benzopyran-2-oneHCID 2924973—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
ProductMethyl 3-(2-(benzyloxy)-5-bromophenyl)-3-phenylpropanoateHCID 21476697—

Reaction Steps

A suspension consisting of (±)-6-bromo-4-phenylchroman-2-one (85.0 g), anhydrous potassium carbonate (46.7 g), sodium iodide (20.5 g) and benzyl chloride (40.6 g) in methanol (350 ml) and acetone (350 ml) was refluxed for 3 hrs. After evaporation of the solvents the residue was extracted with diethyl ether (2×300 ml) and the extract was washed with water (2×200 ml) and aqueous sodium carbonate. Drying (Na2SO4) and rotoevaporation left 121.8 g (102.1% crude yield) of (±)-3-(2-benzyloxy-5-bromophenyl)-3-phenylpropionic acid methyl ester as a light yellow oil, tlc: (1) 0.77; NMR (CDCl3): 39.22, 40.53, 51.63, 70.16, 113.10, 113.77, 126.46, 126.92, 127.88, 128.08, 128.34, 128.45, 130.31, 130.55, 134.41, 136.44, 142.37, 154.94, 172.08.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384980B2
Source datasetuspto-grants-2008_06
ORD IDord-59bb20bc9a4a440d93686a1b203660b0
Source noteuspto-grants-2008_06