Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892033Generated: October 30, 2026

Epichlorohydrin → HCID 86662490, compound

https://huagongshe.com/reaction/1892033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 86662489HCID 86662489—
SolventChloroformHCID 6212—
ProductHCID 86662490HCID 8666249079%

Reaction Steps

As shown in Chemical Formula 2, 3.00 g (12.3 mmol) of 2-(glycidyloxy)-1-naphthoaldehyde oxime (4) was dissolved in 66 mL of chloroform in an ice bath and thereto, 1.84 g (13.5 mmol) of N-chlorosuccinimide (NCS) was added. While stirring the resultant reaction mixture, 1.63 mL (16.0 mmol) of triethylamine was added to the reaction mixture, followed by stirring the resultant reaction mixture for 6 hours to effect the reaction. Then, the reaction solution was washed with each of 50 mL of pure water and 50 mL of Brine three times, and the organic phase was dried over MgSO4, followed by concentrating the solvent under reduced pressure to obtain 2-(glycidyloxy)-1-naphthonitrile oxide B with a yield of 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507611B2
Source datasetuspto-grants-2013_08
ORD IDord-55197c48a20e476ead3ddabe272372fa
Source noteuspto-grants-2013_08