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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398631Generated: October 29, 2026

Boron tribromide → HCID 22315268, compound

https://huagongshe.com/reaction/398631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 22315140HCID 22315140—
SolventDichloromethaneHCID 6344—
ProductHCID 22315268HCID 2231526863.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution 3-cyclopentyl-2-(4-methoxy-phenyl)-N-thiazol-2-yl-propionamide (prepared as in Example 115, 1.03 g, 3.12 mmol) in methylene chloride (31.26 mL) at 25° C. was treated with a 1.0M solution of boron tribromide in methylene chloride (31.26 mL, 31.26 mmol). This solution was stirred at 25° C. for 4 h. At this time, the reaction was cooled to 0° C. and was then quenched by the dropwise addition of a dilute aqueous ammonium hydroxide solution. The resulting solution was stirred at 0° C. for 15 min. This mixture was then poured into water (50 mL) and extracted with ethyl acetate (3×30 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 70/30 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(4-hydroxy-phenyl)-N-thiazol-2-yl-propionamide (626.8 mg, 63.4%) as a off-white solid: mp 198-200° C.; EI-HRMS m/e calcd for C17H20N2O2S (M+) 316.1245 found 316.1256.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610846B1
Source datasetuspto-grants-2003_08
ORD IDord-ced53855b0a845a5b39956f686cc70f9
Source noteuspto-grants-2003_08