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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261389Generated: November 2, 2026

Dimethyl Sulfate → Methyl 3-(1-methyl-2-oxo-2,5-dihydro-1H-pyrrol-3-yl)propanoate

https://huagongshe.com/reaction/2261389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantMethyl 3-(2-oxo-2,5-dihydro-1H-pyrrol-3-yl)propanoateHCID 57443424—
SolventAmmonium ChlorideHCID 25517—
ProductMethyl 3-(1-methyl-2-oxo-2,5-dihydro-1H-pyrrol-3-yl)propanoateHCID 5744342533%

Reaction Steps

0.33 ml of NaHMDS solution (1.0 M in THF, 0.33 mmol) was added to 0.6 ml of THF solution containing 50 mg of 3-(2-oxo-2,5-dihydro-1H-pyrrol-3-yl)-propionic acid methyl ester (2f) (0.30 mmol) prepared by the Step 1 in a dropwise manner at −79° C. and stirred for 30 mins. After 0.3 ml of dimethyl sulfate 0.36 mmol) was added thereto, the reaction mixture was stirred for 4 hrs at 0° C. Then the resulting mixture was dissolved in 2 ml of saturated NH4Cl solution and extracted with 7 ml of ethyl acetate to separate into an organic layer and water layer. The organic layer was washed with 2 ml of saturated NaHCO3 solution and 2 ml of saturated NaCl solution, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resultant was purified by Silica gel column chromatography with EtOAc as an eluant to give 18 mg of 3-(1-methyl-2-oxo-2,5-dihydro-1H-pyrrol-3-yl)-propionic acid methyl ester (2g) (yield: 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846963B2
Source datasetuspto-grants-2010_12
ORD IDord-c31d6509391b418bac4e240730adb956
Source noteuspto-grants-2010_12