HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N-[1-(S)-[alpha-(R)-methoxybenzyl)-3-methyl-butyl]phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-[1-(S)-[alpha-(R)-hydroxybenzyl-]-methylbutyl]phthalimide | HCID 86585458 | — |
| Product | N-[1-(S)-[alpha-(R)-methoxybenzyl)-3-methyl-butyl]phthalimide | HCID 18741230 | — |
Reaction Steps
To a solution of N-[1-(S)-[α-(R)-hydroxybenzyl-]-methylbutyl]phthalimide]30.4 g, 94.0 mmol.) in toluene (380 mL) were successively added methyl p-toluene-sulfonate (19.2 g, 103 mmol) and 60% sodium hydride (4.13 g, 103 mmol.). The resulting mixture was heated under reflux for 18 hours under stirring, cooled to room temperature, successively washed with water and aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by middle pressure column chromatography (n-hexane/ethyl acetate=5/1), to give N-[1-(S)-[α-(R)-methoxybenzyl)-3-methyl-butyl]phthalimide as a white crystalline product (25.6 g, yield: 81%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06689785B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-0dd3c17570f84eb6a2ede9bc4fa40b43 |
| Source note | uspto-grants-2004_02 |