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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076587Generated: October 30, 2026

Water → [2-(Dimethoxymethyl)-3-(methoxymethoxy)-4-(trifluoromethyl)phenyl]methanol

https://huagongshe.com/reaction/2076587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(Dimethoxymethyl)-3-(methoxymethoxy)-4-(trifluoromethyl)benzaldehydeHCID 86617394—
SolventTetrahydrofurfuryl alcoholHCID 7360—
Product[2-(Dimethoxymethyl)-3-(methoxymethoxy)-4-(trifluoromethyl)phenyl]methanolHCID 6711935252%

Reaction Steps

Sodium borohydride (5.11 g, 135 mmol) was added to a solution of crude 2-(dimethoxymethyl)-3-(methoxymethoxy)-4-(trifluoromethyl)benzaldehyde obtained in Example (6-5) in a mixture of tetrahydrofuran-methanol (5:1, 100 ml) under ice-cooling and the mixture was stirred overnight. After the reaction mixture was poured into water and the mixture was extracted with ethyl acetate (four times), the organic layer was successively washed with water (twice) and a saturated aqueous NaCl solution and dried with anhydrous sodium sulfate. The residue obtained by removing the sol-vent under reduced pressure was purified by silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=5/1-2/1) to give [2-(dimethoxymethyl)-3-(methoxymethoxy)-4-(trifluoromethyl)phenyl]methanol as an orange oil (22.6 g, two-step total yield: 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923573B2
Source datasetuspto-grants-2011_04
ORD IDord-d7ca66b528c446aa8aa4087b9e38de6a
Source noteuspto-grants-2011_04