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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217584Generated: October 27, 2026

Pyridine → Benzyl (2,4-difluorophenyl)carbamate

https://huagongshe.com/reaction/217584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,4-DifluoroanilineHCID 9709—
ReactantBenzyl chloroformateHCID 10387—
SolventDichloromethaneHCID 6344—
ProductBenzyl (2,4-difluorophenyl)carbamateHCID 1195452085%

Reaction Steps

To 2,4-difluoro-phenylamine (1, 7.0 mL, 70.0 mmol) in 100 mL of dichloromethane, pyridine (11 mL, 140.0 mmol) and benzyl chloroformate (2, 11.9 mL, 83.4 mmol) were added. The reaction mixture was stirred at room temperature for 1.5 hours. The reaction mixture was concentrated under vacuum and the residue was partitioned between ethyl acetate and potassium bisulfate solution. The organic layer was dried with magnesium sulfate, filtered and the filtrate concentrated under vacuum and crystallized from hexanes to give the desired compound (3, 15.6 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198273B2
Source datasetuspto-grants-2012_06
ORD IDord-484b6415a4ac467fbc16255f4ca732bb
Source noteuspto-grants-2012_06