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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865894Generated: October 25, 2026

Methanol → 4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)benzenemethanol

https://huagongshe.com/reaction/865894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)benzaldehydeHCID 21474525—
SolventWaterHCID 962—
Product4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)benzenemethanolHCID 21474532—

Reaction Steps

1.6 g (5 mmol) of the aldehyde obtained in Example 45, 50 ml of THF and 50 ml of methanol are introduced into a round-bottomed flask. 100 mg (2.5 mmol) of sodium borohydride are added in small portions and the mixture is stirred at room temperature for 4 h. The reaction medium is poured into water, the mixture is extracted with ethyl ether and the organic phase is separated after settling has taken place, dried over magnesium sulphate and evaporated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05567721
Source datasetuspto-grants-1996_10
ORD IDord-c31ca946f76b460aa616114b3d2b0c6d
Source noteuspto-grants-1996_10