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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376426Generated: October 26, 2026

Benzyl chloroformate → 1-Benzyloxycarbonylamino-2-phenylethylphosphonous acid

https://huagongshe.com/reaction/1376426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant1-Amino-2-phenylethylphosponous acidHCID 22916529—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Solvent1,4-DioxaneHCID 31275—
Product1-Benzyloxycarbonylamino-2-phenylethylphosphonous acidHCID 14551341—

Reaction Conditions

Temperature0 °C

Reaction Steps

2.25 ml (14.25 mmol) of benzyl chloroformate are added dropwise, at 0° C. and within the space of 30 min., to a suspension of 1.76 g (9.5 mmol) of 1-amino-2-phenylethylphosponous acid in 15 ml of 1M NaOH, 5 ml of water and 5 ml of dioxane. During a further 2.5 h of stirring at 0° C., the pH of the mixture is maintained at 9-10 using 1M NaOH (approximately 10 ml). After removing the cooling medium, the mixture is stirred at RT overnight. The reaction solution is then washed several times with diethyl ether. The aqueous phase is adjusted to pH 2, at 0°-5° C., using 6M HCl and extracted several times with ethyl acetate. The combined extracts are washed with a saturated solution of NaCl, dried with Na2SO4, filtered and subjected to rotary evaporation i.V. A solid residue remains which is recrystallized from ether/petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663139
Source datasetuspto-grants-1997_09
ORD IDord-d2956f2c407c4e0ab5daa437bf3e87f1
Source noteuspto-grants-1997_09