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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074236Generated: October 25, 2026

Methyl 2,4-dibromobutanoate → 3-hydroxy-1-methylpyrrolidin-2-one

https://huagongshe.com/reaction/1074236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2,4-dibromobutanoateHCID 296716—
Reactant3-hydroxy-1-methylpyrrolidin-2-oneHCID 10313118—
Reactant2,4-Dibromo-N-methylbutanamideHCID 15067983—
Product3-hydroxy-1-methylpyrrolidin-2-oneHCID 10313118—
Product3-Bromo-1-methylpyrrolidin-2-oneHCID 11182954—

Reaction Steps

There is also provided by this invention a method for preparation of 3-hydroxy-N-methylpyrrolidone which comprises conversion of delta-butyrolactone to methyl-2,4-dibromobutyrate, conversion of the methyl-2,4-dibromobutyrate to N-methyl-2,4-dibromobutyramide, ring closure of the N-methyl-2,4-dibromobutyramide to form 3-bromo-N-methyl-2-pyrrolidone, and conversion of the 3-bromo-N-methyl-2-pyrrolidone to 3-hydroxy-N-methyl-2-pyrrolidone by reaction with alkali metal carbonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04973708
Source datasetuspto-grants-1990_11
ORD IDord-3c65bb90c93a406f96f1a224c472a193
Source noteuspto-grants-1990_11