Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581718Generated: October 31, 2026

Epichlorohydrin → N-Butyl-N-[(oxiran-2-yl)methyl]butan-1-amine

https://huagongshe.com/reaction/581718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantDibutylamineHCID 8148—
ProductN-Butyl-N-[(oxiran-2-yl)methyl]butan-1-amineHCID 1240188620.2%

Reaction Steps

A stirred solution of epichlorohydrin (20.0 g, 0.22 mole) is treated dropwise with di-n-butylamine (29.73 g, 0.23 mole) over a 1 hour period followed by continued stirring at room temperature overnight. The reaction mixture is washed with 20% K2CO3 (50 ml). The organic layer is then stirred with 40% NaOH for 1 hour and then extracted with 3×100 ml portions of ether. The etheral extracts are pooled and washed with H2O (100 ml). The organic layer is dried over anhydrous Na2SO4 and filtered. The filtrate is concentrated under reduced pressure to leave the crude product (I) weighing 39.42 g. The crude product is distilled at 52°/0.15 mmHg to give 8.24 g (20.2%) pure product to be used as an intermediate in Part B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922703
Source datasetuspto-grants-1999_07
ORD IDord-0c9cc6dfee794036b6db7416bb43a02b
Source noteuspto-grants-1999_07