HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → (R)-2-benzyl-4-hydroxybutyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | (R)-2-benzylbutyrolactone | HCID 11355800 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-2-benzyl-4-hydroxybutyramide | HCID 53683602 | 63.8% |
Reaction Steps
(R)-2-benzylbutyrolactone (1 gram) was dissolved in 5 ml of absolute ethanol, followed by the addition of 0.5 gram of gaseous ammonia. The solution was kept in a stoppered flask, and the progress of the reaction was followed by thin layer chromatography (eluent dichloromethane/methanol 20:1). After the reaction was judged complete, the ethanol was evaporated and the resulting residue redissolved in ethyl acetate. Ammonia was removed by extraction with 1% HCl, and the ethyl acetate solution was dried over MgSO4, filtered, and rotary evaporated to leave 0.7 grams of (R)-2-benzyl-4-hydroxybutyramide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05916786 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-43059cfc8e174e81af2d4aa5890e9e91 |
| Source note | uspto-grants-1999_06 |