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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833846Generated: October 31, 2026

alpha-Chloro-o-xylene → HCID 12939246, compound

https://huagongshe.com/reaction/1833846

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Chloro-o-xyleneHCID 11093—
ReactantMethyl 2-furoateHCID 11902—
SolventCarbon TetrachlorideHCID 5943—
SolventChloroformHCID 6212—
ProductHCID 12939246HCID 1293924649.2%

Reaction Steps

A mixture of 2-methylbenzyl chloride [prepared as described by Voronkov and Popova, Latv. P.S.R. Zinat. Akad. Vestis Kim. Sev. 1970(5), 595; 62 g.], methyl 2-furoate (114 g.) and anhydrous ferric chloride (1.4 g.) in dry carbon tetrachloride (120 ml.) was heated on a steam bath under relfux for 18 hours. The solution was then evapoated to dryness. The residue was dissolved in chloroform, washed with 2N hydrochloric acid and water, dried over magnesium sulphate and distilled to give methyl 5-(2-methylbenzyl)-2-furoate (50 g.) in the form of a yellow coloured oil, b.p. 140°-170° C./0.1-0.5 mm.Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067723
Source datasetuspto-grants-1978_01
ORD IDord-3f0457abdbf540a4b8843214433509cf
Source noteuspto-grants-1978_01