HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → (R/S)-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | (R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetic acid | HCID 19817647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R/S)-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetic acid | HCID 54389912 | — |
Reaction Steps
4.0 g of (R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetic acid, 80 ml of absolute tetrahydrofuran and 5 ml of acetyl chloride are boiled at reflux for 4 hours while stirring. Thereafter, the mixture is evaporated. The residue is filtered through silica gel (granular size 0.2-0.5 mm). The evaporation residue of the fractions which are eluted with ethyl acetate is stirred in diethyl ether. By filtration there is isolated (R/S)-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetic acid of melting point 95°-96°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04650878 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-f1340adf623b4dadac8a978d029ab879 |
| Source note | uspto-grants-1987_03 |