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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591323Generated: October 31, 2026

Methanol → {4-[2-(Benzyloxy)ethoxy]-3-tert-butoxyphenyl}methanol

https://huagongshe.com/reaction/591323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant4-[2-(Benzyloxy)ethoxy]-3-tert-butoxybenzaldehydeHCID 89156229—
SolventTetrahydrofuranHCID 8028—
Product{4-[2-(Benzyloxy)ethoxy]-3-tert-butoxyphenyl}methanolHCID 70978543—

Reaction Steps

To a stirred mixture of 1.00 g (26.5 mmol) sodium borohydride in 80 ml THF was added 2, 0.9 g (8.83 mmol) 4-[2-(benzyloxy)ethoxy]-3-tert-butoxybenzaldehyde diluted in 40 ml THF drop by drop. The reaction mixture was stirred for 10 min. Methanol (5.8 ml) was added to this mixture drop by drop. The reaction mixture was stirred for 2 hours and poured onto ˜200 ml stirred ice-cooled saturated aqueous ammonium chloride solution. The solution was extracted trice with dichloromethane. The combined organic phases were dried with sodium sulfate and concentrated in vacuo. The crude product was used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238631B2
Source datasetuspto-grants-2016_01
ORD IDord-11d45f88025b4d879dc660c4ca8f9a5a
Source noteuspto-grants-2016_01