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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571472Generated: October 26, 2026

Dichloromethane → 4-bromo-N-[(1R)-1-cyclopropylethyl]-3-fluorobenzamide

https://huagongshe.com/reaction/571472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-3-fluorobenzoic acidHCID 2773341—
Reactant(R)-1-CyclopropylethylamineHCID 7016286—
Product4-bromo-N-[(1R)-1-cyclopropylethyl]-3-fluorobenzamideHCID 7120789295.4%

Reaction Steps

N,N-Diisopropylethylamine (0.92 mL, 5.3 mmol) was added to a mixture of 4-bromo-3-fluorobenzoic acid (0.58 g, 2.6 mmol), (1R)-1-cyclopropylethanamine (0.27 mL, 2.9 mmol, Alfa Aesar: Cat. #H26902) and benzotriazol-1-yloxytris(dimethylamino)-phosphonium hexafluorophosphate (1.3 g, 2.9 mmol) in methylene chloride (5.8 mL, 91 mmol). The reaction mixture was stirred at room temperature for 30 minutes, worked up with aqueous NaHCO3, and extracted with dichloromethylene (3×20 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with ethyl acetate in hexanes (0-10%) to afford the desired product (0.71 g, 94%). LCMS (M+H)+: m/z=286.0/288.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023840B2
Source datasetuspto-grants-2015_05
ORD IDord-734fb3d2bb784c74b8e0a3b0a921da0b
Source noteuspto-grants-2015_05