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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49646Generated: October 30, 2026

Methanol → Dibenzyl L-aspartate

https://huagongshe.com/reaction/49646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPhosphoric AcidHCID 1004—
ReactantSodium HydroxideHCID 14798—
ReactantL-Aspartic acid, 1,4-bis(phenylmethyl) ester, 4-methylbenzenesulfonate (1:1)HCID 2808531—
SolventChloroformHCID 6212—
ProductDibenzyl L-aspartateHCID 2808532—

Reaction Steps

19.4 g of the thus-obtained dibenzyl L-aspartate paratoluenesulfonate was suspended in 150 ml of chloroform, to which was added 16 g (0.04 mols) of aqueous 10% sodium hydroxide solution, and stirred at room temperature for 1 hour. Next, the chloroform layer was separated, to which was added 14.7 g (0.04 mols) of O,O′-diparatoluoyl-L-tartaric anhydride, and again stirred at room temperature for 2 hours. The chloroform layer was analyzed through HPLC. Its chart gave two peaks based on O,O′-diparatoluoyl-L-tartaric acid mono-L-(1,2-dibenzyloxycarbonyl)ethylamide (L-L form) of formula (16) and on O,O′-diparatoluoyl-L-tartaric acid mono-D-(1,2-dibenzyloxycarbonyl)ethylamide (L-D form) of formula (17), and the optical purity of the dibenzyl L-aspartate paratoluenesulfonate used in the reaction was found to be 59.0% ee (FIG. 1—column, CAPCELL PAC SG120; eluent, aqueous phosphoric acid solution (pH 2.2)/methanol=38/62 v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706916B1
Source datasetuspto-grants-2004_03
ORD IDord-9f60f315702d478dbb8a006f304eeacd
Source noteuspto-grants-2004_03