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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678998Generated: October 25, 2026

Benzene → HCID 20364884, compound

https://huagongshe.com/reaction/1678998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
Reactant2-(3-Methylphenyl)-1,3-dioxan-5-olHCID 20364938—
SolventO-XyleneHCID 7237—
ProductHCID 20364884HCID 2036488491.9%

Reaction Steps

A slurry of sodium hydride (2.1 g. 0.08 mole in 100 ml of xylene and 100 ml of benzene was stirred at ambient temperature while 5-hydroxy-2-(3-methylphenyl)-1,3-dioxane (15.9 g, 0.08 mole) was added dropwise during 1 hour. Stirring was continued for one hour and to the mixture was added benzyl chloride (10.4 g, 0.08 mole) during 0.5 hour. This mixture was heated under reflux for 22 hours, cooled, filtered and the filtrate washed with water (2 × 250 ml). The washed solution was dried over magnesium sulfate and concentrated under reduced pressure to give 20.9 g of oil which distilled at 2 × 10-4 mm. to give three fractions distilling respectively at 102°-133° C (cut 1); 133°-141° C (cut 2); and 141° C (cut 3). Analysis of the various cuts indicated that cut 3 was essentially pure cis-5 -benzyloxy-2-(3-methylphenyl)-1,3-dioxane, 2.1 g, m.p. 68°-70° C and this cut was used in further studies.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04077982
Source datasetuspto-grants-1978_03
ORD IDord-d6cb5460598b44559658d2b8eab82672
Source noteuspto-grants-1978_03