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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436329Generated: November 3, 2026

Dichloromethane → HCID 131727774, compound

https://huagongshe.com/reaction/1436329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBoron tribromideHCID 25134—
ReactantHCID 68878932HCID 68878932—
ProductHCID 131727774HCID 131727774—

Reaction Steps

The [3-fluoro-4-(3-methoxy-phenoxy)-benzyl]-(3-methyl-butyl)-amine (460 mg, 1.45 mmol) was dissolved in dichloromethane (10 ml) and cooled to −78° C. as boron tribromide (7.25 mL of a 1.0 M in dichloromethane, 7.25 mmol) was added slowly. After 1 hour at −78° C., the reaction was allowed to warm to room temperature. After 4 hours at room temperature the reaction mixture was carefully being quenched with cold water before the pH was adjusted to 10.0 using concentrated ammonium hydroxide. The reaction mixture was extracted with dichloromethane two times and the combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated. The residue was purified by preparative thin layer chromatography on silica eluting with 5% methanol in ethyl acetate. The HCl salt of the product thus isolated was formed by dissolving the free base in ethyl acetate and adding 1 ml of 4.0 M HCl in dioxane and evaporating to afford the product (2A) a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618996B2
Source datasetuspto-grants-2009_11
ORD IDord-067eec96e98f4d429dc90d5405691528
Source noteuspto-grants-2009_11