Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108550Generated: October 30, 2026

Dichloromethane → HCID 15462730, compound

https://huagongshe.com/reaction/1108550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant4-fluoro-N-hydroxybenzenecarboximidoyl chlorideHCID 2756316—
Reactant4-PentenamideHCID 11815293—
ProductHCID 15462730HCID 15462730—

Reaction Steps

To a flame dried flask containing 4-fluorobenzaldoxime (1.00 g) in DMF (100 mL) is added N-chlorosuccinimide (1.70 g) slowly at 0° C. The reaction is warmed to 50° C. for 3 hours, poured over ice, diluted with H2O(100 mL), and extracted with EtOAc (150 mL). The organic phase is washed with H2O (5×100 mL), saline (100 mL), dried over sodium sulfate, concentrated in vacuo to give a quantitative yield of 4-fluoro-N-hydroxy-benzenecarboximidoyl chloride. To a flask containing 4-fluoro-N-hydroxy-benzenecarboximidoyl chloride (1.25 g) and allyl acetamide (780 mg) in methylene chloride (75 mL) at 0° C. under an inert atmosphere is added triethylamine (3.05 mL, 21.60 mmol). The reaction is slowly warmed to ambient temperature, stirred 20 hours, quenched with water (100 mL), and extracted with methylene chloride (3×100 mL). The organic extracts are combined, washed with saline (50 mL), dried over sodium sulfate, concentrated in vacuo and chromatographed on silica gel (230-400 mesh, 200 mL), eluting with chloroform/methanol (99/1). The appropriate fractions are combined (Rf =0.26, TLC, chloroform/methanol, 95/5) and concentrated in vacuo to give (±)-N-[[4,5-dihydro-3-(4-fluorophenyl)-5-isoxazolyl]methyl]acetamide, mp 167-168° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069141
Source datasetuspto-grants-2000_05
ORD IDord-2314ac8072f84751b3bc02f045982a89
Source noteuspto-grants-2000_05