HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-Pyrrolidinone, 5-(1-methylethoxy)-1-(phenylmethyl)-, (+-)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 15696556 | HCID 15696556 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Pyrrolidinone, 5-(1-methylethoxy)-1-(phenylmethyl)-, (+-)- | HCID 3077960 | 71.2% |
Reaction Steps
To a suspension of 2.5 g of 5-isopropoxy-pyrrolidin-2-one, 1.23 g of potassium hydroxide hydrated to 85%, and 0.25 g of n-tetra-butylammonium bromide in 50 cm3 of tetrahydrofuran, there is added a solution of 2.99 g of benzyl bromide, without exceeding 30° C. After agitating for 1 hour at ambient temperature, the insoluble matter is filtered off and the solvent is evaporated. The residue (4 g) is distilled at 200° C. under 0.05 mbar. The distillate is chromatographed on silica (eluent: ethyl acetate--n-hexane, 1--1). 2.9 g of the expected product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04882350 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-3a58b4b7e1d04ec384e52680f8a28cd1 |
| Source note | uspto-grants-1989_11 |