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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277384Generated: October 30, 2026

Isobutylene oxide → 2-Methyl-1-((4-(4-nitrophenoxy)quinolin-7-yl)oxy)propan-2-ol

https://huagongshe.com/reaction/2277384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylene oxideHCID 11208—
ReactantSodium HydroxideHCID 14798—
Reactant4-(4-Nitrophenoxy)quinolin-7-olHCID 136350299—
SolventWaterHCID 962—
Product2-Methyl-1-((4-(4-nitrophenoxy)quinolin-7-yl)oxy)propan-2-olHCID 6819425742.7%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a flask containing 4-(4-nitrophenoxy)quinolin-7-ol (14.45 g, 45.33 mmol) was added a solution of sodium hydroxide (3.63 g, 90.66 mmol) in water/95% EtOH (90 mL/10 mL) followed by isobutylene oxide (12.12 mL, 136 mmol, pre-cooled to 0° C.). After stirring at 45° C. for 10 minutes, more isobutylene oxide (12.12 mL, 136 mmol, pre-cooled to 0° C.) was added. The reaction was continued to stir for additional 12 hours. The mixture was cooled to room temperature and continued to stir for 4 hours, then cooled to 0° C. and stirred for additional 10 minutes. The resulted solid was filtered, and then dissolved in DCM (130 mL). The solution was filtered and concentrated in vacuo. The residue was washed with petroleum ether (30 mL), and dried in vacuo at 45° C. overnight to afford the title compound as a yellow solid (6.86 g, 42.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133162B2
Source datasetuspto-grants-2015_09
ORD IDord-70c6776d94694798a3aa9559fd275461
Source noteuspto-grants-2015_09