Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170030Generated: November 1, 2026

Isopropanol → 5-Bromo-2-(1-methylethoxy)pyridine

https://huagongshe.com/reaction/2170030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-2-chloropyridineHCID 2734414—
Product5-Bromo-2-(1-methylethoxy)pyridineHCID 2193506878%

Reaction Conditions

Temperature60 °C

Reaction Steps

60% NaH in oil (1.5:1, Sodium hydride:Mineral Oil, 5.20 g) was added in two portions to isopropyl alcohol (150 mL) at room temperature under N2. The mixture was stirred at 60° C. for 30 min. 5-bromo-2-chloropyridine (10.00 g, 51.96 mmol) was added in two portions and the mixture was stirred at reflux 4 h and than at 80° C. overnight. The solution was concentrated in vacuo. Water (50 mL) and EtOAc (50 mL) was added and the layers were separated. The aqueous layer was extracted with EtOAc (50 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered and the solvent was removed in vacuo. The crude product was subjected to flash chromatography (silica, 0-50% EtOAc in heptanes) to give the title compound as a clear oil (8.74 g, 78%). 1H NMR (600 MHz, DMSO) δ 8.17 (s, 1H), 7.61 (dd, 1H), 6.59 (d, 1H), 5.23 (m, 1H), 1.33 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050327B2
Source datasetuspto-grants-2015_06
ORD IDord-049ed4f286584ba1981b215b1306dcfb
Source noteuspto-grants-2015_06