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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721071Generated: October 30, 2026

Dimethyl Sulfate → Methyl (2S)-1-methyl-5-oxoprolinate

https://huagongshe.com/reaction/1721071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantMethyl 5-oxo-L-prolinateHCID 78646—
SolventDiethyl EtherHCID 3283—
ProductMethyl (2S)-1-methyl-5-oxoprolinateHCID 12361160—

Reaction Conditions

Temperature60 °C

Reaction Steps

The methyl ester compound from step 5a above (18.3 kg, 127.8 mol) and dimethyl sulfate (20.09 kg, 159.3 mol) were introduced into a reactor, and the mixture was heated to 60° C. under an N2 atmosphere. Heating was continued until the concentration of starting material dropped below 15%. An additional 6.25 kg (0.5 eq) of dimethyl sulfate was added with exothermic response. The thick reaction mixture was then cooled to 25° C., and a solution of triethylamine (16.12 kg) in diethyl ether (19.2 L) was added at such a rate that the temperature did not rise above 30° C. The emulsion was washed with two 50 L portions of water. The ether layer was separated, and the residue was extracted with ethyl acetate (60 l). The combined organic layers were dried over Na2SO4 and azeotroped with toluene until no more triethylamine remained in the residue. The residue was mixed with dimethyl sulfate (1.7 kg, 13.5 mol) and THF (70 L) and refluxed under nitrogen until the reaction was complete. The solvents were evaporated under vacuum, and the residue was distilled under high vacuum to yield a colorless product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508418
Source datasetuspto-grants-1996_04
ORD IDord-d9c7f2c6b8da4a12ad23bfa6009307f7
Source noteuspto-grants-1996_04