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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248557Generated: October 30, 2026

Sodium Thiosulfate → 2-Methoxymethyloxy-4,5,6-trimethoxyphenol

https://huagongshe.com/reaction/248557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Methoxymethyloxy-4,5,6-trimethoxybenzaldehydeHCID 20095708—
SolventDichloromethaneHCID 6344—
Product2-Methoxymethyloxy-4,5,6-trimethoxyphenolHCID 20095709—

Reaction Steps

12.8 g of 2-methoxymethyloxy-4,5,6-trimethoxybenzaldehyde prepared in Referential Example 11 was dissolved in 100 ml of dichloromethane, and 8.7 g of m-chloroperbenzoic acid was added thereto at room temperature while stirring. The mixture was refluxed for 30 min and cooled with ice, and 100 ml of a saturated aqueous sodium thiosulfate solution was added thereto. The precipitated crystals were separated by filtration. The mother liquor was washed with a saturated aqueous sodium hydrogen-carbonate solution, dried over anhydrous magnesium sulfate and concentrated. The residue was mixed with 50 ml of ethanol, 40 ml of water and 21.3 g of potassium hydroxide, and the mixture was stirred for 1 hr under reflux. The reaction mixture was cooled, poured into dilute hydrochloric acid and extracted with ethyl acetate. The organic phase was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off to prepare 11.5 g of the product compound (light yellow oleaginous) as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210239
Source datasetuspto-grants-1993_05
ORD IDord-a9d4fd00379c45f0b1a834239e7a8aa7
Source noteuspto-grants-1993_05