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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390589Generated: October 30, 2026

Sodium borohydride → HCID 67128148, compound

https://huagongshe.com/reaction/2390589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86646365HCID 86646365—
SolventMethanolHCID 887—
ProductHCID 67128148HCID 67128148—

Reaction Steps

A solution of 2.5g (10.49 mmol) 2-fluoro-5-(tetrahydropyrane-2-yloxymethyl)-benzaldehyde in anhydrous methanol is mixed in portions with 0.60 g (15.7 mmol) sodium borohydride while stirring and stirred for another hour at room temperature. After adding water, extraction is performed using diethyl ether, and the organic phase is dried over sodium sulfate. After removing the solvent under vacuum, the benzyl alcohol is obtained in pure form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273793B2
Source datasetuspto-grants-2012_09
ORD IDord-15fb6455c09b4dc99b2d741003aacf09
Source noteuspto-grants-2012_09