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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278018Generated: November 2, 2026

Benzyl Alcohol → {6-[(Benzyloxy)methyl]-1,4-dioxan-2-yl}methanol

https://huagongshe.com/reaction/1278018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantDiglycidyl etherHCID 16704—
ReactantSodiumHCID 5360545—
SolventWaterHCID 962—
Product{6-[(Benzyloxy)methyl]-1,4-dioxan-2-yl}methanolHCID 5400488620.1%

Reaction Steps

108 g of benzyl alcohol (1.0 mole) is stirred under a nitrogen atmosphere at room temperature and 0.4 g of sodium is added to the mixture and stirring continued for 2-1/2 hours. Then 13.1 g of 2,2'-(oxybismethylene)bisoxirane (0.1 mole) is added and the mixture then heated to reflux for 18 hours. The mixture is then cooled to room temperature and with stirring is poured into 350 ml of water. The aqueous mixture is extracted with 2×200 ml portions of chloroform, the CHCl3 extracts are combined and dried over anhydrous sodium sulfate. The CHCl3 is removed in vacuo and the resulting yellow oil then vacuum distilled through a 10 cm vigreux column. The fraction distilling at 150°-154° @0.4 mm is collected yielding 4.8 g (20%) of the above compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04279902
Source datasetuspto-grants-1981_07
ORD IDord-bdfb172dd63344a1a76e90c60281b246
Source noteuspto-grants-1981_07