HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 2(S)-[2-phenyl-1(S)-phthalimidoethyl]oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | methanesulfonic acid (2S,3S)-3-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-2-hydroxy-4-phenylbutyl ester | HCID 56626679 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2(S)-[2-phenyl-1(S)-phthalimidoethyl]oxirane | HCID 10266388 | 61.3% |
Reaction Steps
A solution of 0.26 g of methanesulfonic acid (2S,3S)-3-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-2-hydroxy-4-phenylbutyl ester in 1.6 ml of tetrahydrofuran is treated at -15° with a solution of 0.090 g of potassium tertbutylate in 0.5 ml of tetrahydrofuran and the mixture is stirred for 0.5 hours. The mixture is treated with 2.2 ml of semi-saturated sodium chloride solution and the pH value is adjusted to 6 with 0.1 ml of 1N sulphuric acid. Thereafter, the mixture is extracted with ethyl acetate. The extracts are dried and filtered, and the filtrate is evaporated to give 0.12 g (60%) of 2(S)-[2-phenyl-1(S)-phthalimidoethyl]oxirane, IR (KBr): 1773m and 1709s (C=O of imide).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05641886 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-a042ce57d2ee498f8a5c6dbd5249b893 |
| Source note | uspto-grants-1997_06 |