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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347676Generated: October 30, 2026

Water → 4-[(6-Chloro-3-pyridazinyl)oxy]benzenemethanol

https://huagongshe.com/reaction/347676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 17859705HCID 17859705—
SolventMethanolHCID 887—
Product4-[(6-Chloro-3-pyridazinyl)oxy]benzenemethanolHCID 1785971376%

Reaction Steps

3-Chloro-6-(4-formylphenoxy)pyridazine (4.06 g, 17.3 mmol) and 200 mL of methanol were mixed, and after sodium borohydride (654 mg, 17.3 mmol) was added under cooling with ice and stirring, the mixture was stirred for 15 minutes. Water was added to the reaction mixture and methanol was distilled off. The residue was poured into water, which was extracted with ethyl acetate. The extracted solution was washed with saturated brine, then dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel chromatography (eluate n-hexane:ethyl acetate=1:2 v/v) to obtain 3.10 g (76%) of the title compound as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176204B2
Source datasetuspto-grants-2007_02
ORD IDord-dadae83fcd9645f797ee40cdeb618f20
Source noteuspto-grants-2007_02