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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459161Generated: November 1, 2026

Benzyl Bromide → HCID 23295265, compound

https://huagongshe.com/reaction/1459161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant(2,2-Dimethyl-1,3-dioxan-5-yl)methanolHCID 3584869—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 23295265HCID 2329526572%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-hydroxymethyl-2,2-dimethyl-1,3-dioxane (cf:Bates, H. A.; Farina, J.; Tong, M. J. Org. Chem. 1986, 51, 2637, 3.0 g, 20.5 mmol) in 25 mL of dry DME under argon was added via cannula to a slurry of NaH (0.740 g, 80% dispersion in oil, 24.6 mmol) in 60 mL of dry DME cooled to 0° C. The resulting grey slurry was stirred at room temperature for 0.5 h, then recooled to 0° C., and treated with a solution of benzylbromide (4.56 g, 26.7 mmol) in 20 mL of DME. The reaction mixture was stirred at room temperature (rt) overnight and then quenched with 100 ml of H2O. The aqueous layer was separated and extracted with two portions of ethyl acetate. The combined organic layers were then washed with saturated sodium chloride solution, dried over MgSO4, filtered, and concentrated to provide a yellow oil. Purification by column chromatography on silica gel (ethyl acetate/hexane) afforded 3.51 g (72%) of 5-benzyloxymethyl-2,2-dimethyl-1,3-dioxane as a clear colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854228
Source datasetuspto-grants-1998_12
ORD IDord-9de05460a02a4e81a6d4a39f9e92f123
Source noteuspto-grants-1998_12