HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085452Generated: October 31, 2026
Triethylamine → ((2R)-2-phenylpropyl)[(methylethyl)sulfonyl]amine
https://huagongshe.com/reaction/2085452
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 2-Propanesulfonyl chloride | HCID 82408 | — |
| Reactant | (R)-(+)-beta-Methylphenethylamine | HCID 1547949 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | ((2R)-2-phenylpropyl)[(methylethyl)sulfonyl]amine | HCID 11481889 | 92% |
Reaction Steps
To a solution of the (2R)-2-phenylpropylamine (1.2g, 8.87mmol) in hexane (16.0 mL) was added triethylamine (2.47 mL, 17.74 mmol) and dimethylaminopyridine (0.30 g, 2.47 mmol). Cooled reaction to 5° C., then added a solution of isopropylsulfonyl chloride (0.97 mL, 8.69 mmol) dissolved in methylene chloride (6.0 mL) over a period of 15.0 minutes. Stirred for 45.0 minutes, then stirred at room temperature for 120.0 minutes. Quenched reaction with IN HCl (20.0 mL) and extracted organic with methylene chloride (25.0 mL). Dried organic layer with anhydrous magnesium sulfate, filtered and concentrated filtrate to provide the final title compound, ((2R)-2-phenylpropyl)[(methylethyl)sulfonyl]amine, (1.93 g, 90.1%) an oil; 1H nmr (CDCl3, 300 MHz) δ 1.25 (d, 3H, J=6.9Hz), 1.29(d, 3H, J=6.9Hz), 1.30 (d, 3H, J=7.2 Hz), 2.98 (m, 1H), 3.05 (m, 1H), 3.22 (m, 1H), 3.36 (m, 1H), 3.89 (b, 1H), 7.23 (m, 2H), 7.34 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06720357B2 |
|---|
| Source dataset | uspto-grants-2004_04 |
|---|
| ORD ID | ord-1295869916a84999809be9b534370de8 |
|---|
| Source note | uspto-grants-2004_04 |
|---|