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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744749Generated: October 28, 2026

Citric Acid → Cbz-L-Phenylalaninal

https://huagongshe.com/reaction/744749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantN-carbobenzoxy-L-phenylalanilolHCID 853481—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductCbz-L-PhenylalaninalHCID 7021150—

Reaction Conditions

Temperature-60 °C

Reaction Steps

A solution of 24.5 ml of anhydrous dimethyl sulfoxide in 870 ml of anhydrous dichloromethane was cooled under N2 atmosphere to -60° C. and treated over a period of 15 min with 131 ml of a 2M solution of oxalyl chloride in dichloromethane in order that the internal temperature remained below -50° C. After addition, the solution was stirred at -60° C. for 15 min and treated over a period of 20 min with a solution of 50 g (0.175 mol) of N-(((benzyl)oxy)-carbonyl)-L-phenylalaninol in 200 ml of dichloromethane. The resulting solution was stirred at -60° C. for 1 h, then treated over a period of 15 min with 97 ml of triethylamine in order that the internal temperature remained below -50° C. After addition the solution was stirred at -60° C. for 15 min, then, with the cooling bath in place, was treated rapidly (over a period of 1 min) with a solution of 163 g of citric acid in 550 ml of water. The resulting slurry was stirred vigorously for 10 min, allowed to warm, diluted to 1 liter with water, and separated. The organic layer was washed with 700 ml of water followed by a mixture of 550 ml of water and 150 ml of saturated aqueous NaHCO3, dried over MgSO4, and concentrated in vacuo at 20° C. to give the crude desired compound as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559158
Source datasetuspto-grants-1996_09
ORD IDord-0b51f8cb454f481ea7f69f451aafdd14
Source noteuspto-grants-1996_09