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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420856Generated: November 2, 2026

2-Bromopropane → 5-Benzyloxy-2-isopropoxynitrobenzene

https://huagongshe.com/reaction/1420856

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Benzyloxy)-2-nitrophenolHCID 4606634—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Benzyloxy-2-isopropoxynitrobenzeneHCID 1878260599%

Reaction Conditions

Temperature50 °C

Reaction Steps

2-Bromopropane (4.51 mL, 5.90 g, 48 mmol) was added to a mixture of 4-benzyloxy-2-nitrophenol (J.Biol.Chem., 1985, 260, 3440, 2.94 g, 12 mmol) and potassium carbonate (9.95 g, 72 mmol) in dimethylformamide (20 mL) and the mixture was stirred at 50° C. for 22 h. The mixture was cooled, diluted with water (100 mL) and extracted with ethyl acetate (3×100 mL). The combined organic fractions were washed with aqueous sodium hydroxide (1M, 4×100 mL) and brine (100 mL), dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound as an orange oil (3.40 g, 99%). 1H NMR (360 MHz, CDCl3) δ 7.41-7.33 (6H, m), 7.12 (1H, dd, J 9.1, 3.1 Hz), 7.02 (1H, d, J 9.1 Hz), 5.05 (2H, s), 4.52 (1H, hept, J 6.1 Hz), and 1.35 (6H, d, J 6.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071927
Source datasetuspto-grants-2000_06
ORD IDord-57bf91a6b0cb4e08b0aac83d573304ba
Source noteuspto-grants-2000_06