Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361865Generated: October 31, 2026

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

https://huagongshe.com/reaction/2361865

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 numberUS08691814B2
Source datasetuspto-grants-2014_04
ORD IDord-d06f7c3d257840238353f3738c910c42
Source noteuspto-grants-2014_04