Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433309Generated: October 26, 2026

1-(Chloromethyl)-2-iodobenzene → (3-Formyl-4-(2-iodo-benzyloxy)-phenyl)-acetic acid methyl ester

https://huagongshe.com/reaction/1433309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Chloromethyl)-2-iodobenzeneHCID 101064—
Reactant2-NaphthylalanineHCID 185915—
ReactantMethyl 2-(3-formyl-4-hydroxyphenyl)acetateHCID 12374099—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
Product(3-Formyl-4-(2-iodo-benzyloxy)-phenyl)-acetic acid methyl esterHCID 11682982—

Reaction Steps

A solution of (3-formyl-4-hydroxy-phenyl)-acetic acid methyl ester (17.2 g, 85.9 mmol) in acetonitrile was slowly added to a solution of 1-chloromethyl-2-iodo-benzene (13.06 g, 94.5 mmol) and Nal (3.22 g, 21.5 mmol) in acetonitrile (273 ml) at reflux temperature and the mixture was mantained at this temperature for 3 hours. Once the mixture reached room temperature, the residue that had formed was filtered, washed with acetonitrile and concentrated to obtain a residue that was then dissolved in toluene (330 ml) and washed with NaOH 0.1N and water. The organic layer was concentrated to dryness, diluted with acetone (330 ml) and was stirred into water (500 ml) at room temperature. The mixture was filtered and washed with water to obtain 33.959 (96%) of [3-Formyl-4-(2-iodo-benzyloxy)-phenyl]-acetic acid methyl ester, which was purified by crystallization in toluene-cyclohexane (99% HPLC)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612219B2
Source datasetuspto-grants-2009_11
ORD IDord-6cdb77fceeb14b63b7ac2bc4f30fd8f5
Source noteuspto-grants-2009_11