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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075962Generated: October 25, 2026

Imidazole, 5-(2-chloroethyl)-1-methyl-2-nitro- → 1-ME-2-NO2-5-Vinyl imidazole

https://huagongshe.com/reaction/1075962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazole, 5-(2-chloroethyl)-1-methyl-2-nitro-HCID 90183—
ReactantPotassium tert-butoxideHCID 23665647—
SolventBenzeneHCID 241—
Product1-ME-2-NO2-5-Vinyl imidazoleHCID 93215—

Reaction Steps

To a solution of 18.9 g. of 5-(2-chloroethyl)-1-methyl-2-nitroimidazole (prepared according to the procedure of British Pat. No. 1,222,486) in 2.8 liters of anhydrous benzene cooled to 5°-10° C., 16.8 g. of potassium tert-butoxide is added. Stirring is continued for 2 hours at 5°-10° C. After filtration and concentration to dryness under vacuum at a temperature lower than 50° C., the resulting yellow oily residue is washed three times with 50 ml. of ethyl ether (or light petroleum). The title product is obtained, which is dried under vacuum at 40° C.; yield 12 g. (77.7%). A sample crystallized from ethyl ether melts at 106°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954789
Source datasetuspto-grants-1976_05
ORD IDord-1dc4c2dcbd484499bf4d0d95e7d51419
Source noteuspto-grants-1976_05