HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2,4-dibromobutanoate → 3-hydroxy-1-methylpyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2,4-dibromobutanoate | HCID 296716 | — |
| Reactant | 3-hydroxy-1-methylpyrrolidin-2-one | HCID 10313118 | — |
| Reactant | 2,4-Dibromo-N-methylbutanamide | HCID 15067983 | — |
| Product | 3-hydroxy-1-methylpyrrolidin-2-one | HCID 10313118 | — |
| Product | 3-Bromo-1-methylpyrrolidin-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04973708 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-3c65bb90c93a406f96f1a224c472a193 |
| Source note | uspto-grants-1990_11 |