Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413548Generated: October 30, 2026

N-methyl-2-pyrrolidone → HCID 12148789, compound

https://huagongshe.com/reaction/413548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl N-methylaminoacetate hydrochlorideHCID 171173—
ReactantHCID 12148787HCID 12148787—
SolventWaterHCID 962—
ProductHCID 12148789HCID 1214878943%

Reaction Conditions

Temperature92.5 °C

Reaction Steps

To a 125 mL round-bottomed flask equipped with condenser and nitrogen inlet were added 486 mg (1.20 mmol) 3-phenyl-3-[4-(3-trifluoromethyl-phenoxy)-phenoxy]-1-chloropropane, 184 mg (1.20 mmol) sarcosine ethyl ester hydrochloride, 0.416 mL (2.40 mmol) diisopropylethylamine, and 6 mL dry N-methylpyrrolidinone. The reaction was heated at 90-95° C. for 60 h, cooled, and poured into water. After extracting with ethyl acetate, the organic layer was washed with water (3 times) and brine, dried over sodium sulfate, and evaporated. The residue was chromatographed on silica gel using methylene chloride/methanol as eluant to afford 250 mg (43%) of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566550B2
Source datasetuspto-grants-2003_05
ORD IDord-9710c24986b741fdb39be5849545c0ab
Source noteuspto-grants-2003_05