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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645310Generated: October 29, 2026

Benzyl chloroformate → Benzyl [4-(benzyloxy)-3-fluorophenyl]carbamate

https://huagongshe.com/reaction/1645310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant1-(Benzyloxy)-2-fluoro-4-nitrobenzeneHCID 22030912—
CatalystPlatinumHCID 23939—
SolventEthyl AcetateHCID 8857—
ProductBenzyl [4-(benzyloxy)-3-fluorophenyl]carbamateHCID 57754845—

Reaction Steps

A mixture of 34.9 g of 1-benzyloxy-2-fluoro-4-nitrobenzene (WO 03 064413) (MW: 247.28, 141 mmol) and 340 mg of platinum (5% on activated carbon) in 350 ml of ethyl acetate was stirred at RT and normal pressure under a hydrogen atmosphere. The course of the reaction was monitored by HPLC and the reaction was terminated after 20 h. The catalyst was filtered off and the filtrate was concentrated to dryness under reduced pressure using a rotary evaporator. The oily residue was dissolved in 500 ml of acetone and 250 ml of a saturated sodium hydrogen carbonate solution and 17.5 g of sodium hydrogen carbonate (MW: 84.01, 208 mmol) were added. The mixture was cooled to 5° C. and 26.08 g of benzyl chloroformate (MW: 170.59, 152 mmol) were added dropwise. The mixture was then stirred for 2 h at RT and the course of the reaction was monitored by TLC (hexane/ethyl acetate 3:1). The acetone was removed under reduced pressure, 500 ml of water were added to the residue, and the solid material was filtered off. The crystals were washed with 500 ml of water and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124772B2
Source datasetuspto-grants-2012_02
ORD IDord-fd5998b5f87a4609921e891df7662174
Source noteuspto-grants-2012_02