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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095756Generated: October 31, 2026

2-Methoxyethanol → 2-Chloro-4-(2-methoxyethoxy)pyridine

https://huagongshe.com/reaction/1095756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
Reactant2-Chloro-4-nitropyridineHCID 735152—
ReactantPotassium tert-butoxideHCID 23665647—
Product2-Chloro-4-(2-methoxyethoxy)pyridineHCID 6377757797.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 2-chloro-4-nitropyridine (43.6 g, 275 mmol) and 2-methoxyethanol (325 ml, 425 mmol) was cooled to 0° C. Potassium 2-methylpropan-2-olate (35.7 g, 302 mmol) was added and the resulting mixture was stirred while warming to ambient temperature over 2 hours. The reaction mixture was concentrated under reduced pressure followed by dilution with 500 ml of water. The resulting mixture was extracted with dichloromethane. The combined organic layers were dried over MgSO4 and concentrated under reduced pressure to produce the desired compound as an oil (50.2 g). MS APCI (+) m/z 188 and 189.9 (M+1 of each isotope) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138181B2
Source datasetuspto-grants-2012_03
ORD IDord-ed2cce96f47245f3aedbacff5e86bf67
Source noteuspto-grants-2012_03