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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178334Generated: November 1, 2026

Pyridine → HCID 58696288, compound

https://huagongshe.com/reaction/1178334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic acid, 2-chloro-2,2-difluoro-, 1,1'-anhydrideHCID 76074—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58696296HCID 58696296—
SolventDichloromethaneHCID 6344—
ProductHCID 58696288HCID 5869628846%

Reaction Steps

tert-Butyl[1-(3,4-dichlorophenyl)-1-methylaminomethyl-3-butenyl]methylcarbamate (500 mg) produced in Example 4 was dissolved in methylene chloride (10 mL). Under cooling with ice, pyridine (163 μL) and chlorodifluoroacetic acid anhydride (350 μL) were added thereto. Under cooling with ice, the mixture was stirred for 50 minutes. Saturated aqueous sodium bicarbonate was added to the reaction mixture, and the resultant mixture was extracted with methylene chloride. The organic layer was washed with saturated brine, dried over sodium sulfate anhydrate, and concentrated under reduced pressure. The residue was purified through silica gel column chromatography (n-hexane:ethyl acetate=4:1), to thereby give the title compound (300 mg, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276511B2
Source datasetuspto-grants-2007_10
ORD IDord-0158647d2a52410983b5da4e75c88e14
Source noteuspto-grants-2007_10