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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271659Generated: November 2, 2026

Alanine methyl ester hydrochloride → HCID 87830865, compound

https://huagongshe.com/reaction/1271659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAlanine methyl ester hydrochlorideHCID 2733257—
ReactantHydroxybenzenesulfonic acidHCID 15619088—
SolventMethyl AcetateHCID 6584—
ProductHCID 87830865HCID 87830865—

Reaction Steps

L-Ala-OMe HCl salt (1.00 g, 7.16 mmol) was suspended in methyl acetate (15 ml), and benzenesulfonic acid monohydrate (BsOH H2O) (1.51 g, 8.57 mmol) was added. The mixture was stirred for dissolution. This solution was concentrated under reduced pressure, and methyl acetate (15 ml) was added. The mixture was concentrated twice under reduced pressure, and the obtained concentrate was cooled in a refrigerator. Since partial crystallization occurred, diethyl ether (3 ml) and methyl acetate (15 ml) were added to dissolve the crystals almost entirely at 40° C. This solution was stirred at room temperature and cooled overnight in a refrigerator. The crystals were separated and dried to give L-alanine methyl ester benzenesulfonate (L-Ala-OMe BsOH salt) crystals. The crystals were left standing at room temperature for a while. As a result, the crystals were liquefied and failed to provide stable crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205433B2
Source datasetuspto-grants-2007_04
ORD IDord-a6c4c991277f457bb6108fd023fea4c5
Source noteuspto-grants-2007_04