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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187285Generated: October 29, 2026

Pyridine → Benzyl (2,4-difluorophenyl)carbamate

https://huagongshe.com/reaction/1187285

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 (30, 7.0 mL, 70.0 mmol) in 100 mL of dichloromethane, pyridine (11 mL, 0.14 mol) and benzyl chloroformate (31, 11.9 mL, 83.4 mmol) are added. The reaction mixture is stirred at ambient temperature for 1.5 hours. The reaction mixture is concentrated under vacuum and the residue is partitioned between ethyl acetate and potassium bisulfate solution. The organic layer is dried with magnesium sulfate, filtered, and the filtrate concentrated under vacuum. The resulting material is crystallized from hexanes to provide the desired compound (32, 15.6 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673928B2
Source datasetuspto-grants-2014_03
ORD IDord-7b50e0b8e6ee4460a6de76c0dd33449b
Source noteuspto-grants-2014_03