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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329503Generated: October 29, 2026

Hydrogen Peroxide → HCID 13982256, compound

https://huagongshe.com/reaction/329503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantBoraneHCID 6331—
ReactantSodium HydroxideHCID 14798—
Reactant2H-Pyran, 3,4-dihydro-6-[(phenylmethoxy)methyl]-HCID 11356175—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13982256HCID 13982256—

Reaction Steps

A 1M solution of borane in 29.3 ml of tetrahydrofuran was added dropwise to a solution of 9.00 g of 6-benzyloxymethyl-3,4-dihydro-2H-pyran (prepared as described in Preparation 1) dissolved in 30 ml of tetrahydrofuran at a temperature, whilst maintaining the temperature in the range from -5° C. to 0° C. The reaction mixture was then stirred at room temperature for 3 hours, after which a 10% w/v aqueous solution of sodium hydroxide was added dropwise. 10.8 ml of 30% v/v aqueous hydrogen peroxide were then added, whilst keeping the temperature in the range from 32° to 40° C. The mixture was then stirred for a further 1 hour at room temperature, after which the organic layer was separated, washed wth water, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The oily residue (10.5 g) was purified by column chromatography through 250 g of silica gel. 8.82 g of the title compound were obtained from those fractions eluted with a 1:20 by volume mixture of ethyl acetate and methylene chloride. It boiled at 130°-135° C. (bath temperature)/1 mmHg (133 Pa).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04891363
Source datasetuspto-grants-1990_01
ORD IDord-21d2326a17fe49288cddc32b9f49d060
Source noteuspto-grants-1990_01