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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252023Generated: November 1, 2026

Triethylamine → N-(2,3-Epoxypropyl)-N-ethylaniline

https://huagongshe.com/reaction/252023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-(N-ethylanilino)propane-1,2-diolHCID 458693—
ReactantSodium MethoxideHCID 10942334—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductN-(2,3-Epoxypropyl)-N-ethylanilineHCID 8919245%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methanesulfonyl chloride (2.5 mL, 1.5 eq.) was added to a solution 3-(ethyl-phenyl-amino)-propane-1,2-diol (4.22 g, 21.6 mmol) and triethylamine (9.03 mL, 3.0 eq.) in dichloromethane (20 mL) at −30 to −35° C. and the resulting mixture was stirred and warmed to 0° C. The reaction was quenched by sat. NaHCO3 (30 mL) and the separated aqueous phase was extracted with 2×20 mL CH2Cl2 and 20 mL EtOAc. The combined extracts were dried over Na2SO4, filtered and concentrated. The residue was dissolved in MeOH (30 mL) and treated with NaOMe (2.3 g, 2.0 eq.) at 65-70° C. for 3 h. After cooling to room temperature, the mixture was diluted with sat. NaHCO3 (50 mL) and extracted with 3×30 mL of EtOAc. The combined extracts were dried over Na2SO4, filtered and concentrated and the product was purified by chromatography (10% EtOAc/hexanes) to give ethyl-oxiranylmethyl-phenyl-amine (1.72 g, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868002B2
Source datasetuspto-grants-2011_01
ORD IDord-6b53e76e84a34f08a9efecd2449051ff
Source noteuspto-grants-2011_01