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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364725Generated: October 26, 2026

Allyl bromide → Benzyl 3-allyloxy-4-nitro-benzoate

https://huagongshe.com/reaction/2364725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Hydroxy-4-nitrobenzoic acid benzyl esterHCID 14986435—
SolventAcetonitrileHCID 6342—
ProductBenzyl 3-allyloxy-4-nitro-benzoateHCID 6810711594.2%

Reaction Steps

Benzyl 3-hydroxy-4-nitro-benzoate 29a (4.50 g, 16.47 mmol) was dissolved in 75 mL of anhydrous acetonitrile. The resulting solution was added with potassium carbonate (6.83 g, 49.41 mmol) and 3-bromopropene (2.9 mL, 32.94 mmol) successively, heated to reflux for 3 hours, then filtered. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound benzyl 3-allyloxy-4-nitro-benzoate 29b (4.86 g, yield: 94.2%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-53317d265ba04b569e60309df7e53e78
Source noteuspto-grants-2014_04