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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276252Generated: October 30, 2026

Methanol → Leucine methyl ester hydrochloride

https://huagongshe.com/reaction/276252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantL-LeucineHCID 6106—
ReactantThionyl ChlorideHCID 24386—
ProductLeucine methyl ester hydrochlorideHCID 272369586%

Reaction Steps

To a suspension of (L)-leucine, (315 g, 2.4 mol) in MeOH (3.2 L) at −15° C. was added SOCl2 (315 mL, 4.32 mol, 1.8 equiv.) dropwise at such a rate that the temp. of the reaction did not exceed 5° C. After the addition was complete, the reaction mixture was allowed to warm to room temp. and was stirred overnight. The resulting mixture was concentrated under reduced pressure and Et2O (3 L) was slowly added to the residue to produce a precipitate. The mixture was cooled with an ice bath, then treated with additional MeOH (3 L) relatively rapidly. After 1 h at 0° C., the crystals were collected and dried to give (L)-leucine methyl ester HCl salt as a white crystalline solid (394 g, 86%): mp 147-149° C.; 1H-NMR (CD3OD) δ0.78-0.98 (m, 6 h), 1.58-1.72 (m, 3H), 3.76 (g, 3H), 3.92 (t, J=7.3 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353006B1
Source datasetuspto-grants-2002_03
ORD IDord-1e61807dc0d84b88ad8238f010ba58d6
Source noteuspto-grants-2002_03