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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419271Generated: October 30, 2026

Tetrahydrofuran → HCID 54261585, compound

https://huagongshe.com/reaction/2419271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Methylphenoxy)-5-methyl-benzoic acidHCID 13738055—
SolventBenzeneHCID 241—
ProductHCID 54261585HCID 54261585—

Reaction Steps

A solution of 121 g. of 2-(4-methyl-phenoxy)-5-methyl-benzoic acid in 600 ml. of tetrahydrofuran is slowly added dropwise, with cooling in an icebath, to 420 ml. of a 70% solution of sodium dihydro-bis(1-methoxyethoxy)-aluminate in benzene and stirred for an additional hour at room temperature. To the obtained clear solution, 800 ml. of 20% aqueous sodium hydroxide solution are carefully added dropwise. Then, the organic phase is separated. The aqueous phase is extracted three additional times with ether. The organic extracts are washed with saturated sodium chloride solution and the latter dried over sodium sulfate. After evaporation of the ether, there is obtained 2-(4-methylphenoxy)-5-methyl-benzyl alcohol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105664
Source datasetuspto-grants-1978_08
ORD IDord-24296600da2f48d98719e7d6a2f2bf4c
Source noteuspto-grants-1978_08