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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904280Generated: October 31, 2026

3-(methoxymethyl)pyridine → HCID 14553814, compound

https://huagongshe.com/reaction/1904280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(methoxymethyl)pyridineHCID 338926—
ReactantHCID 14553813HCID 14553813—
ProductHCID 14553814HCID 1455381420%

Reaction Steps

3-Methoxymethylpyridine (1.75 g) was added to 3-(m-phenoxyphenyl)-2-methylpropyl iodide (1.0 g) at room temperature, and the resultant mixture was stirred at 120° C. for 4 hours. The reaction mixture was cooled to room temperature and washed with diethyl ether three times. Methanol (20 ml) was added thereto, and after addition of sodium borohydride (0.21 g) at room temperature, the resultant mixture was stirred at the same temperature for 15 hours. The resultant mixture was admixed with water (200 ml) and 15% aqueous sodium hydroxide solution (20 ml) and extracted with diethyl ether (50 ml×3). The extracts were combined together, washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography to give N-[3-(m-phenoxyphenyl)-2-methylpropyl]-3-methoxymethyl-1,2,5,6-tetrahydropyridine (0.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837236
Source datasetuspto-grants-1989_06
ORD IDord-fba7abe601e343db81cc14b42e686569
Source noteuspto-grants-1989_06