Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413382Generated: November 2, 2026

Phosphate → (4S,5R)-1,3-dibenzyl-5-methoxycarbonyl-2-oxoimidazolidine-4-carboxylic acid

https://huagongshe.com/reaction/2413382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantDimethyl cis-1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylateHCID 11234411—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product(4S,5R)-1,3-dibenzyl-5-methoxycarbonyl-2-oxoimidazolidine-4-carboxylic acidHCID 1115284391.4%

Reaction Conditions

Temperature30 °C

Reaction Steps

To a suspension of dimethyl cis-1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylate (10.0 g) in a mixture of 0.1m phosphate buffer (pH 8.0, 900 ml) and methanol (100 ml) was added Pig Liver Esterase (manufactured by Sigma Lab., 32000 units, 200 mg). The mixture was stirred at 30° C. for 42 hours while the pH was adjusted to around 8.0 with 1 N aqueous sodium hydroxide solution. Chloroform (500 ml) was added to the mixture. Then, the mixture was adjusted to pH 2 with diluted sulfuric acid. The aqueous and chloroform layers were separated. The chloroform layer was washed with water, dried over anhydrous magnesium sulfate and concentrated to give (4S,5R)-1,3-dibenzyl-5-methoxycarbonyl-2-oxoimidazolidine-4-carboxylic acid (8.80 g). M.P., 145°-147° C. [α]36520 =-25.3° (c=1, DMF).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04496739
Source datasetuspto-grants-1985_01
ORD IDord-063ef84cdb1c4aecb16063cc4749fdae
Source noteuspto-grants-1985_01