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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571617Generated: November 1, 2026

Benzyl Alcohol → HCID 68284297, compound

https://huagongshe.com/reaction/571617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68284875HCID 68284875—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 68284297HCID 6828429799%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(2,6-diethyl-4-methylphenyl)-6-methoxymethoxymethyl-5-(4-methylphenylsulfonyl)-2-methyl-3(2H)-pyridazinone (2.38 g, 4.91 mmol) and benzylalcohol (797 mg, 7.37 mmol) in dry DMF (10 ml) was added 60% sodium hydride (294 mg, 7.35 mmol) at 5° C. The reaction solution was stirred at 0° C. for 1 hour. The reaction solution was diluted with water, and extracted with tert-butyl methyl ether 2 times. The combined organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to give 2.12 g of 4-(2,6-diethyl-4-methylphenyl)-6-methoxymethoxymethyl-5-benzyloxy-2-methyl-3(2H)-pyridazinone (yield: 99%) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029295B2
Source datasetuspto-grants-2015_05
ORD IDord-12254ee38f934c2c8409028446461a3d
Source noteuspto-grants-2015_05