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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303980Generated: October 27, 2026

Water → 1-p-Toluenesulfonyl-2(r)-ethylaziridine

https://huagongshe.com/reaction/2303980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-1-butanolHCID 22129—
Solventtert-Butyl methyl etherHCID 15413—
Product1-p-Toluenesulfonyl-2(r)-ethylaziridineHCID 11009637—

Reaction Conditions

Temperature25 °C

Reaction Steps

R-(−)-2-amino-1-butanol (99.96 g, 105 mL) and tert-butyl methyl ether (TBME) (277 g, 366 mL) are combined under a nitrogen atmosphere. This mixture is stirred for several minutes and 10 N aqueous sodium hydroxide (449 mL) is added over a period of about 10 minutes. The reaction mixture is cooled to below 10° C. and a solution of p-toluene sulfonyl chloride (TsCl) (464 g) in TBME (711 g) is added over a period of about 50 minutes, maintaining the temperature of the reaction mixture at or below 32° C. After the addition is complete, the mixture is stirred for about 30 minutes at 40° C., and water (900 mL) is added while cooling the mixture to 25° C. The layers are separated and the organic layer washed sequentially with water (150 g) and 25% aqueous sodium chloride solution (300 g). Toluene (450 g) is added to the organic layer, and the mixture distilled under reduced pressure, maintaining the temperature of the mixture at or below 45° C., until the water content of the mixture is below about 0.1%. The resulting solution is used, without further treatment, for the preparation described in Example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433172B1
Source datasetuspto-grants-2002_08
ORD IDord-767678e1701641d28b66beb8adacdeea
Source noteuspto-grants-2002_08