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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271655Generated: November 2, 2026

L-Alanine → HCID 10063562, compound

https://huagongshe.com/reaction/1271655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-AlanineHCID 5950—
Reactant2,5-Dimethylbenzenesulfonic acidHCID 11868—
SolventEthanolHCID 702—
ProductHCID 10063562HCID 10063562123%

Reaction Conditions

Temperature70 °C

Reaction Steps

L-alanine (1.50 g, 16.84 mmol) and 2,5-dimethylbenzenesulfonic acid (2,5-DMBS) (3.76 g, 20.20 mmol) were added to ethanol (15 ml), and the mixture was heated overnight at 70° C. to perform esterification. To complete the esterification reaction, the mixture was heated to 90° C., and ethanol (200 ml) was added over 3.5 hours, while distilling away almost the same amount of ethanol. Thereafter, the solvent was evaporated under reduced pressure, and the residue was dried under reduced pressure. The obtained oily residue was cooled in a refrigerator to allow partial crystallization. Ethyl acetate (7 ml) was added, and the residue was dissolved almost entirely at 50° C. The mixture was stirred at room temperature, diethyl ether (40 ml) was further added, and the mixture was stirred at room temperature to give a slurry. The obtained slurry was cooled overnight in a refrigerator, and the crystals were separated and dried to give 3.77 g of L-alanine ethyl ester 2,5-dimethylbenzenesulfonate (L-Ala-OEt 2,5-DMBS salt) dry crystals (L-Ala-OEt 2,5-DMBS salt content 95.6%,11.88 mmol, yield 70.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205433B2
Source datasetuspto-grants-2007_04
ORD IDord-39876a7fbb624d0a9dcb3f373af3c8f2
Source noteuspto-grants-2007_04