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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891946Generated: October 26, 2026

Hydrochloric Acid → (5-Methoxypyridazin-3-yl)methanol

https://huagongshe.com/reaction/891946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23600258HCID 23600258—
SolventEthanolHCID 702—
Product(5-Methoxypyridazin-3-yl)methanolHCID 2224019283.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Methoxy-pyridazine-3-carboxylic acid ethyl ester (8.1 g, 44.5 mmol) was dissolved in ethanol (105 ml) under argon. The reaction mixture was cooled to 0° C. and treated with NaBH4 (3.5 g, 89 mmol). After 10 minutes, the reaction mixture was warmed to room temperature, stirred for 1 hour and treated successively with 2N HCl and saturated sodium bicarbonate to adjust the pH at 8. The solvent was removed in vacuo and the residue was stirred with MeOH (100 ml). The suspension was filtered and the filtrate was concentrated. The residue was chromatographed over silica gel (CH2Cl2—MeOH 19:1) to provide (5-methoxy-pyridazin-3-yl)-methanol (5.2 g, 83%) as a light brown solid, MS: m/e=140 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005432B2
Source datasetuspto-grants-2006_02
ORD IDord-f6aeae6adc7f4e68a6cb71a2ab701636
Source noteuspto-grants-2006_02