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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072929Generated: October 30, 2026

Triethylamine → HCID 14390522, compound

https://huagongshe.com/reaction/2072929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-3-nitropyridineHCID 79613—
ReactantMethyl D-alaninate hydrochlorideHCID 11182647—
SolventMethanolHCID 887—
ProductHCID 14390522HCID 143905225.9%

Reaction Steps

A suspension of 2-chloro-3-nitropyridine (37.76 g, 0.239 mole), (R)-alanine methyl ester hydrochloride (50 g, 0.358 mole) and triethylamine (60.3 g, 0.597 mole) in methanol (370 ml) was refluxed overnight under nitrogen. The solvents were removed under reduced pressure and the resulting solid was triturated in ethyl acetate (300 ml), filtered, and rinsed with additional ethyl acetate. The filtrate and washings were combined and washed once with water. The aqueous wash was extracted with ethyl acetate and the combined organic layers were washed several times with water, dried over sodium sulfate, filtered and evaporated under reduced pressure to given an oil weighing 45.6 g (85%). Elution of a portion of the oil with 1:6 tetrahydrofuran/hexane through a silica gel column gave 3.2 g of product after evaporation of solvent. Drying of a portion of the solid under high vacuum at room temperature gave 0.98 g of title compound, mp 39°-40° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914109
Source datasetuspto-grants-1990_04
ORD IDord-8a1c52d543744ad49746d728d9da9ddd
Source noteuspto-grants-1990_04