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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764398Generated: November 1, 2026

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

https://huagongshe.com/reaction/1764398

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 numberUS04116669
Source datasetuspto-grants-1978_09
ORD IDord-698cc70c582b4367bc762d658949b9f6
Source noteuspto-grants-1978_09