HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → (S)-3-(m-tolylamino)-1-phenylpropan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | m-Toluidine | HCID 7934 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (S)-3-hydroxy-3-phenylpropyl 4-methylbenzenesulfonate | HCID 11449624 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-3-(m-tolylamino)-1-phenylpropan-1-ol | HCID 58200036 | 57% |
Reaction Steps
To a solution of the (S)-3-hydroxy-3-phenylpropyl 4-methylbenzenesulfonate (100 mg, 0.33 mmol) in anhydrous acetonitrile (2 mL) were added K2CO3 (91 mg, 0.66 mmol), NaI (12 mg, 0.0825 mmol) and m-toluidine (42 mg, 0.39 mmol). The mixture was refluxed overnight. The mixture was filtered, and the filter cake was washed with EtOAc. The filtrate was concentrated to give the crude product, which was purified by preparative TLC (3:1 Petroleum ether/EtOAc) to give (S)-3-(m-tolylamino)-1-phenylpropan-1-ol (45 mg, 57%). 1H NMR (400 MHz, CDCl3): δ=2.05 (m, 2H), 2.25 (s, 3H), 3.25 (m, 2H), 3.40 (s, 2H), 4.90 (m, 1H), 6.50 (m, 4H), 7.05 (m, 1H), 7.30 (m, 1H), 7.40 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598160B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-cbbbc380277d44fb96c95b9bb8bfab4e |
| Source note | uspto-grants-2013_12 |