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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70720Generated: October 26, 2026

Triethylamine → HCID 67398270, compound

https://huagongshe.com/reaction/70720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
Reactant(4-Tert-butylphenyl)(5-chloro-6-methoxypyridin-2-yl)methanolHCID 67396476—
SolventCyclohexaneHCID 8078—
ProductHCID 67398270HCID 6739827096%

Reaction Steps

Sulfuryl chloride (0.37 mL) was added to a solution of (4-tert-butylphenyl)(5-chloro-6-methoxypyridin-2-yl)methanol obtained in Example 7-4(1) (200 mg) and triethylamine (0.27 mL) in cyclohexane (4 mL) at room temperature, and then the mixture was stirred at the same temperature for 17 hours. After completion of the reaction, the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=20:1) to give 6-[(4-tert-butylphenyl)(chloro)methyl]-3-chloro-2-methoxypyridine as a colorless oil (203 mg, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822503B2
Source datasetuspto-grants-2014_09
ORD IDord-0c602aa7de284ba0b7a9193426a57181
Source noteuspto-grants-2014_09