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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581719Generated: October 31, 2026

Epichlorohydrin → HCID 12401887, compound

https://huagongshe.com/reaction/581719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantDiisobutylamineHCID 8085—
ProductHCID 12401887HCID 1240188737.14%

Reaction Steps

A stirred solution of epichlorohydrin (21.0 g, 0.23 mole) is treated dropwise with diisobutylamine (31.14 g, 0.24 mole) over a 1 hour period followed by continuous 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 with the organic layer 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. The crude product is distilled at 68°/0.1 mmHg to yield 15.83 g (37.14%) pure product to oe used as an intermediate in Part B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922703
Source datasetuspto-grants-1999_07
ORD IDord-5b4b775743624b858ebdcdf517385ce0
Source noteuspto-grants-1999_07