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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526050Generated: October 30, 2026

Toluene → Methyl 1-(2-cyanophenyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/526050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1,2-DibromoethaneHCID 7839—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl(2-cyanophenyl)acetateHCID 1512623—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
ProductMethyl 1-(2-cyanophenyl)cyclopropanecarboxylateHCID 5947061865.3%

Reaction Steps

1.5 g of tetra-n-butylammonium bromide, 6.5 g of 1,2-dibromoethane and 20 mL of aqueous 50% sodium hydroxide solution were added to a toluene (40 mL) solution of 4.0 g of methyl 2-cyanophenylacetate, and stirred at room temperature for 1 hour. Water was added to the reaction liquid, and extracted with ethyl acetate. The organic layer was washed with saturated saline water, dried with anhydrous magnesium sulfate, and the solvent was evaporated away under reduced pressure. The crude product was purified through silica gel column chromatography (hexane/ethyl acetate) to obtain 3.0 g of the entitled compound as a colorless compound. 1H-NMR (400 MHz, CDCl3) δ: 7.66 (1H, dd, J=7.6, 1.2 Hz), 7.55 (1H, td, J=7.6, 1.2 Hz), 7.43-7.36 (2H, m), 3.66 (3H, s), 1.82 (2H, q, J=3.7 Hz), 1.30 (2H, q, J=3.7 Hz) ESI-MS Found: m/z [M+H] 202.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345705B2
Source datasetuspto-grants-2016_05
ORD IDord-a1101ced932b48f3987eeadbcb6c7fef
Source noteuspto-grants-2016_05