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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965639Generated: October 25, 2026

Iodine → (+/-)-N-[2-chloro-3-[[4-chloro-3-(trifluoromethyl)phenyl]hydroxymethyl]phenyl]acetamide

https://huagongshe.com/reaction/965639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-2-chloro-alpha,alpha,alpha-trifluorotolueneHCID 67959—
ReactantN-(2-chloro-3-formylphenyl)acetamideHCID 22312916—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-N-[2-chloro-3-[[4-chloro-3-(trifluoromethyl)phenyl]hydroxymethyl]phenyl]acetamideHCID 2231292274.5%

Reaction Conditions

Temperature32.5 °C

Reaction Steps

A solution of 4-bromo-1-chloro-2-(trifluoromethyl)benzene (0.165 mol) in THF (30 ml) was added dropwise under N2 flow to a suspension of Mg (0.181 mol) and a crystal of I2 in THF (20 ml). The mixture was stirred at 30-35° C. for 2.5 hours and then cooled to 10° C. The mixture was added dropwise at 5° C. under N2 flow to a solution of N-(2-chloro-3-formylphenyl)acetamide (0.0788 mol) in THF (500 ml). The mixture was stirred at RT for 3 hours, poured out into ice and NH4Cl, and extracted with EtOAc. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography (eluent: CH2Cl2/CH3OH 98.5/1.5). The pure fractions were collected and the solvent was evaporated, yielding 22.2 g (74%) of (±)-N-[2-chloro-3-[[4-chloro-3-(trifluoromethyl)phenyl]hydroxymethyl]phenyl]acetamide (interm. 25).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951857B2
Source datasetuspto-grants-2005_10
ORD IDord-84adc887521541ecaeb6939ef33be814
Source noteuspto-grants-2005_10