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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant2-Propanesulfonyl chlorideHCID 82408—
Reactant(R)-(+)-beta-MethylphenethylamineHCID 1547949—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product((2R)-2-phenylpropyl)[(methylethyl)sulfonyl]amineHCID 1148188992%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720357B2
Source datasetuspto-grants-2004_04
ORD IDord-1295869916a84999809be9b534370de8
Source noteuspto-grants-2004_04