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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418735Generated: November 3, 2026

Citric Acid → HCID 11235137, compound

https://huagongshe.com/reaction/1418735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantDimethyl SulfoxideHCID 679—
ReactantEthyl AcetateHCID 8857—
ReactantSodium amideHCID 24533—
ReactantBenzyl N,N-dibenzyl-L-phenylalaninateHCID 10928230—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11235137HCID 1123513785.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

3.76 g (96.39 mmol) of sodium amide was suspended in 40 ml of dimethylsulfoxide and heated at from 74° to 75° C. for 30 minutes. 40 ml of tetrahydrofuran was added to the resulting solution and cooled to 0° C. To this was dropwise added a solution of 15.47 g (90.5 wt. %, 32.14 mmol) of N,N-dibenzyl-(L)-phenylalanine benzyl ester as dissolved in 20 ml of tetrahydrofuran, while keeping it at 0° C. After these were reacted at 0° C. for 30 minutes, 120 ml of an aqueous solution of 10% citric acid and 100 ml of ethyl acetate were added to the reaction mixture, which was thus subjected to phase separation. The aqueous layer thus separated was extracted once with 50 ml of ethyl acetate, and the resulting extract was combined with the previously-separated organic layer and then washed with 60 ml of a saturated saline solution. This was dried with anhydrous sodium sulfate, filtered and concentrated, and the resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=from 2/1 to 1/3) and then crystallized in toluene/hexane to obtain 11.16 g of the above-entitled compound. The yield was 85.6%. The integral ratio in 1H-NMR of the compound verified that the ratio of the diastereomers constituting it is about 1:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883284
Source datasetuspto-grants-1999_03
ORD IDord-5500b0f61daa465c8c37eb77e752915f
Source noteuspto-grants-1999_03