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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270097Generated: October 26, 2026

Iodine → HCID 57608017, compound

https://huagongshe.com/reaction/270097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Benzyl-3-pyrrolidinoneHCID 69890—
Reactant2-(Bromomethyl)-4-chloro-1-fluorobenzeneHCID 2773626—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductHCID 57608017HCID 57608017—

Reaction Steps

To a stirring suspension of magnesium strip (1.39 g, 57.06 mmol) in diethyl ether (10 mL) was added a crystal iodine followed by 0.5 mL of 2-(bromomethyl)-4-chloro-1-fluorobenzene under nitrogen. The reaction was initiated with a high intensity heat gun, then a solution of 2-(bromomethyl)-4-chloro-1-fluorobenzene (12.75 g, 57.06 mmol) in diethyl ether was added at such a speed that gentle reflux was maintained. After addition was complete the reaction mixture was kept on stirring at reflux for 3.5 h, cooled to room temperature and a solution of 1-benzylpyrrolidin-3-one (10.0 g, 57.06 mmol) in diethyl ether (20 mL) was added dropwise with vigorous stirring. After addition was complete the reaction mixture was left overnight at room temperature. This reaction mixture was treated with aqueous ammonium chloride (NH4Cl) solution and extracted with ethyl acetate. The organic layer was washed with water, dried over sodium sulphate (Na2SO4), filtered, concentrated and the residue was purified by silica gel flash chromatography (0-2% methanol in dichloromethane, 0.2% ammonium hydroxide, NH4OH) to give the subtitled compound (650 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449475B2
Source datasetuspto-grants-2008_11
ORD IDord-bdc88208e02f45d4b6962f92ff71c766
Source noteuspto-grants-2008_11