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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782193Generated: November 3, 2026

Dichloroacetyl chloride → HCID 57588411, compound

https://huagongshe.com/reaction/1782193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloroacetyl chlorideHCID 6593—
ReactantTriethylamineHCID 8471—
ReactantHCID 57588493HCID 57588493—
SolventDichloromethaneHCID 6344—
ProductHCID 57588411HCID 57588411—

Reaction Steps

tert-Butyl 2-(3-(3-(2,6-dichlorophenyl)isoxazol-5-yl)phenylamino)ethylcarbamate (230 mg, 0.51 mmol) was dissolved in anhydrous dichloromethane with triethylamine (120 μL, 0.82 mmol). The mixture was cooled in an ice-bath under nitrogen, then a solution of dichloroacetyl chloride (120 mg, 0.82 mmol) was added dropwise. After the addition was completed the ice-bath was removed and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with dichloromethane and then washed successively with water, 10% hydrochloric acid and saturated sodium bicarbonate solution. The organic solution was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by flash column chromatography, on silica gel, eluting with 95:5 hexanes:ethyl acetate to yield tert-butyl 2-(2,2-dichloro-N-(3-(3-(2,6-dichlorophenyl)isoxazol-5-yl)phenyl)acetamido)ethylcarbamate. 1H NMR (CDCl3): 7.99 (d, 1H), 7.82 (br s, 1H), 7.62 (m, 1H), 7.48-7.30 (m, 4H), 6.78 (s, 1H), 5.82 (s, 1H), 4.95 (m, 1H), 3.95 (m, 2H), 3.43 (m, 2H), 1.42 ppm (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498353B2
Source datasetuspto-grants-2009_03
ORD IDord-17d7fafd1516472bab6b2d77e50431b9
Source noteuspto-grants-2009_03