HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2S)-2-(phenoxymethyl)oxirane → (S)-N-(2-[2-hydroxy-3-phenoxypropyl]aminoethyl)isobutyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2S)-2-(phenoxymethyl)oxirane | HCID 1534345 | — |
| Reactant | N-(2-Aminoethyl)-2-methylpropanamide | HCID 12681828 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-N-(2-[2-hydroxy-3-phenoxypropyl]aminoethyl)isobutyramide | HCID 10493020 | 46% |
Reaction Steps
A mixture of (S)-1,2-epoxy-3-phenoxypropane (0.495 g.) and N-(2-aminoethyl)isobutyramide (0.429 g) in ethanol (25 ml) was heated under reflux for 48 hours. The reaction mixture was cooled and solvent removed by rotary evaporation in vacuo. The residual solid was purified by column chromatography on silica (Merck, Art. 7736) using 5% v/v methanol in dichloromethane as eluant. The solid thereby obtained was purified by recrystallisation from ethyl acetate to give (S)-N-(2-[2-hydroxy-3-phenoxypropyl]aminoethyl)isobutyramide (0.425 g), m.p. 88°-89° C., 24 [α]D -5.8° [c, 1.04; methanol], mixed m.p. with material from Example 1, 88°-89° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04764361 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-d6361fc02bb54f1c9603ccba5ef42389 |
| Source note | uspto-grants-1988_08 |