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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081875Generated: November 1, 2026

Sodium borohydride → 2-Methoxymethoxy-5-(trifluoromethyl)benzyl alcohol

https://huagongshe.com/reaction/1081875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-(Methoxymethoxy)-5-(trifluoromethyl)benzaldehydeHCID 23363113—
SolventMethanolHCID 887—
Product2-Methoxymethoxy-5-(trifluoromethyl)benzyl alcoholHCID 5438838295%

Reaction Steps

The solution of 2-methoxymethoxy-5-(trifluoromethyl)benzaldehyde (3.3 g) from Example 59 in anhydrous methanol (20 ml) was cooled in an ice bath, followed by gradual addition of NaBH4 (0.53 g). After stirring at room temperature for 15 minutes, the solvent was removed under reduced pressure. To the residue was added water, and the aqueous layer was extracted with ether. The ether layer was washed with water and saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, to give an colorless oil compound as the title compound (3.15 g; 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587392
Source datasetuspto-grants-1996_12
ORD IDord-5890f8f66af04e2d9ebcf9b627454dbe
Source noteuspto-grants-1996_12