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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247898Generated: October 31, 2026

Pyridine → Decylamine

https://huagongshe.com/reaction/247898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroformHCID 6212—
ReactantDichloromethaneHCID 6344—
ReactantSodium BicarbonateHCID 516892—
ReactantDiboronHCID 6328200—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventTriethylamineHCID 8471—
Solvent1,4-DioxaneHCID 31275—
ProductDecylamineHCID 8916—

Reaction Steps

An alternative synthesis of 10 can be accomplished by first reacting the amine 6 with a suitable carboxylic acid (as a melt) or with an acid chloride in an inert solvent such as methylene chloride, chloroform, ether or toluene and with a base such as triethylamine, pyridine or sodium bicarbonate present. The intermediate amide is then reduced with a suitable reagent such as diborane in an inert solvent such as ether, tetrahydrofuran (THF), dioxane or dimethoxyethane to afford the desired amine 10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05208252
Source datasetuspto-grants-1993_05
ORD IDord-bfd6fac7dafe43f0b928d2622cad077d
Source noteuspto-grants-1993_05