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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52168Generated: October 26, 2026

3-(Chloromethyl)pyridine hydrochloride → 3-(Diethoxyphosphorylmethyl)pyridine

https://huagongshe.com/reaction/52168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
ReactantTriethyl phosphiteHCID 31215—
ReactantSodium BicarbonateHCID 516892—
Product3-(Diethoxyphosphorylmethyl)pyridineHCID 1046260526.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of saturated NaHCO3 was added 3-picolyl chloride hydrochloride (8.2 g, 50 mmol). After gas evolution ended, the mixture was extracted with CH2Cl2. The organic phase was dried (MgSO4) and concentrated in vacuo. To the resulting residue was added triethylphosphite (8.3 g, 50 mmol) and the neat mixture was stirred and heated at 85° C. overnight. The mixture was cooled and purified by flash column chromotography on silica gel eluting with 5% MeOH--CH2Cl2 to afford 3.0 g of diethyl 3-pyridylmethylphosphonate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616596
Source datasetuspto-grants-1997_04
ORD IDord-3480f0481a594e518e4e31c7f928693f
Source noteuspto-grants-1997_04