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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294103Generated: October 27, 2026

Ethanol → (2-Benzyloxy-5-methoxymethoxyphenyl)methanol

https://huagongshe.com/reaction/1294103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Benzyloxy-5-methoxymethoxybenzaldehydeHCID 17861251—
SolventWaterHCID 962—
Product(2-Benzyloxy-5-methoxymethoxyphenyl)methanolHCID 1786129499.8%

Reaction Steps

To a mixture of 2-benzyloxy-5-methoxymethoxybenzaldehyde (10.03 g), ethanol (50 mL) and tetrahydrofuran (100 mL) was added sodium tetrahydroborate (1.43 g) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added water and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated to give (2-benzyloxy-5-methoxymethoxyphenyl)methanol as a colorless oil (10.08 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-216d3aabc43a42bf84ce93a06b49a3db
Source noteuspto-grants-2007_07