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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374993Generated: October 30, 2026

Diisopropyl Ether → (3-methoxy-4-methylphenyl)methanol

https://huagongshe.com/reaction/1374993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
Reactant2-Methoxy-4-methylbenzoic acidHCID 597164—
ReactantSodium borohydrideHCID 4311764—
ReactantBoronHCID 5462311—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(3-methoxy-4-methylphenyl)methanolHCID 11744818—

Reaction Steps

A solution of 3-methoxy-p-toluic acid (45.32 g) in tetrahydrofuran (280 ml) was added to a suspension of sodium borohydride (9.29 g) in tetrahydrofuran (45 ml) with ice bath cooling under nitrogen atmosphere. After 10 minutes stirring, boron trifuluoride diethyl etherate (41.5 ml) was added to the mixture at 3 to 15° C. and the whole was stirred at room temperature overnight. Water (210 ml) and diisopropyl ether (60 ml) were added to the mixture. The organic layer was separated and the aqueous layer was extracted with diisopropyl ether (100 ml). The combined organic layer was washed successively with 1N sodium hydroxide solution and brine, dried over sodium sulfate, and evaporated in vacuo to give 3-methoxy-4-methylbenzylalcohol (41.63 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166598B2
Source datasetuspto-grants-2007_01
ORD IDord-0e7d7a21a9264f86ace7ff2698ee528b
Source noteuspto-grants-2007_01