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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329502Generated: October 30, 2026

Water → 2H-Pyran, 3,4-dihydro-6-[(phenylmethoxy)methyl]-

https://huagongshe.com/reaction/329502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
Reactant(3,4-Dihydro-2H-pyran-6-yl)methanolHCID 12511647—
SolventDimethylformamideHCID 6228—
Product2H-Pyran, 3,4-dihydro-6-[(phenylmethoxy)methyl]-HCID 1135617592%

Reaction Steps

A solution of 5.71 g of 6-hydroxymethyl-3,4-dihydro-2H-pyran dissolved in 100 ml of dimethylformamide was added dropwise to a mixture of 2.18 g of sodium hydride (as a 55% w/w dispersion in mineral oil) and dimethylformamide, whilst ice-cooling. The mixture was then stirred at room temperature for 1 hour, after which 6.33 g of benzyl chloride were added to it. The mixture was stirred for 16 hours, after which it was poured into 1 liter of water. The resulting mixture was then extracted twice with ethyl acetate. The combined extracts were washed with water, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The oily residue (13 g) was subjected to column chromatography through 200 g of silica gel. 9.40 g of the title compound were obtained as a colorless oil from those fractions eluted with mixtures of diethyl ether and hexane ranging from 4:100 to 5:100 by volume. It boiled at 125°-130° C. (bath temperature)/1 mmHg (133 Pa).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04891363
Source datasetuspto-grants-1990_01
ORD IDord-6e4af5ddfc164d82987515a31354fa1c
Source noteuspto-grants-1990_01