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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358423Generated: October 30, 2026

Epichlorohydrin → HCID 13239942, compound

https://huagongshe.com/reaction/358423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium hydrideHCID 24758—
ReactantHCID 604309HCID 604309—
ProductHCID 13239942HCID 1323994297%

Reaction Steps

2.1 g (6.6 mmol) of N-α-methylbenzyl-2-nitrobenzenesulfonamide was dissolved in 10 ml of epichlorohydrin, to which was gradually added at room temperature 0.35 g (7.3 mmol) of 50% sodium hydride, followed by agitating at room temperature for 30 minutes and reacting under reflux for 1 hour. The epichlorohydrin was distilled off under reduced pressure, water was added and extracted with ethyl acetate. The ethyl acetate phase was dried over anhydrous magnesium sulfate, concentrated, and purified by the silica gel chromatography to obtain the intended product (Compound No. 33). The yield was 97% and the nD26.5 value was 1.5572. The results of the elemental analysis are shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04468245
Source datasetuspto-grants-1984_08
ORD IDord-4a1e3e3dbe90403daa02509876296502
Source noteuspto-grants-1984_08