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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913939Generated: October 30, 2026

2-(Dimethylamino)ethanol → HCID 70497649, compound

https://huagongshe.com/reaction/1913939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
ReactantMethyl 4,5,6-trichloropicolinateHCID 12993691—
ReactantHCID 178418750HCID 178418750—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70497649HCID 70497649—

Reaction Steps

A 100 mL three-neck flask equipped with a reflux condenser and nitrogen inlet was charged with methyl 4,5,6-trichloropicolinate (2.40 g, 9.98 mmol). Anhydrous THF (50 mL) was added followed by N,N-dimethylethanolamine (0.20 g). The reaction mixture was sparged with nitrogen for 15 min. Solid Pd(PPh3)2Cl2 (140 mg, 0.2 mmol) was added. The reaction mixture was stirred under nitrogen for 20 min. Diethylzinc (1 M solution in hexanes; 10 mL, 10 mmol) was added in 2 mL portions. When starting material was no longer observed through analysis by GC, the reaction mixture was quenched with water and extracted into EtOAc. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated under reduced pressure to a white solid (2.34 g). Analysis by GC-MS showed the solid contained 11% starting methyl 4,5,6-trichloropicolinate. 1H NMR (400 MHz, CDCl3) δ 8.06 (s, 1H, pyridine H), 4.01 (s, 3H, CO2Me), 3.10 (q, J=8 Hz, 2H, CH2), 1.33 (t, J=8 Hz, 3H, CH2CH3); 13C{1H} NMR (101 MHz, CDCl3) δ 164.4, 162.8, 145.4, 143.3, 132.9, 124.5 (C3), 53.1 (CO2Me), 30.0 (CH2), 12.3 (CH2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609855B2
Source datasetuspto-grants-2013_12
ORD IDord-fddfd33d38c84c539562ceffd740c393
Source noteuspto-grants-2013_12