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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443677Generated: October 30, 2026

alpha-Chloro-o-xylene → HCID 12884120, compound

https://huagongshe.com/reaction/443677

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Chloro-o-xyleneHCID 11093—
ReactantSodium hydrideHCID 24758—
Reactant(2,5,5-Trimethyl-tetrahydro-furan-2-yl)-methanolHCID 12634236—
SolventTolueneHCID 1140—
ProductHCID 12884120HCID 1288412080%

Reaction Steps

2,5,5-Trimethyl-2-hydroxymethyl tetrahydrofuran (1.6 g) was added slowly to a stirred suspension of sodium hydride (0.4 g of 80% dispersion in oil) in dry toluene (55 ml). After the addition the mixture was heated under reflux for 1 hour. 2-Methylbenzyl chloride (1.8 g) was added and the mixture heated under reflux overnight. The cooled mixture was washed with water (x2) and dried and the solvent was removed under reduced pressure. The product was purified by chromatography on silica using methylene dichloride as eluent. Yield 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE030574
Source datasetuspto-grants-1981_04
ORD IDord-31a0d20491b14ed286272cdd3e4cf655
Source noteuspto-grants-1981_04