Reaktion #1173963

ord-c84d61d8a20e4afe9083ce44fa6606f8

Reaktionsgleichung

COC(=O)C(Br)CCBr
methyl-2,4-dibromobutyrate
CNC(=O)C(Br)CCBr
N-methyl-2,4-dibromobutyramide
CNC(=O)C(Br)CCBr
N-methyl-2,4-dibromobutyramide
CN1CCC(O)C1=O
3-hydroxy-N-methylpyrrolidone
COC(=O)C(Br)CCBr
methyl-2,4-dibromobutyrate
CN1CCC(Br)C1=O
3-bromo-N-methyl-2-pyrrolidone
CN1CCC(O)C1=O
3-hydroxy-N-methyl-2-pyrrolidone

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThere is also provided by this invention a method

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05032402uspto-grants-1991_07