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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826686Generated: October 31, 2026

Pentane → (2-Aminophenyl)(3-methoxyphenyl)methanone

https://huagongshe.com/reaction/1826686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
ReactantTetrahydrofuranHCID 8028—
Reactant2-BromoanisoleHCID 11358—
Reactant2-AminobenzonitrileHCID 72913—
ReactantHCID 178418306HCID 178418306—
Product(2-Aminophenyl)(3-methoxyphenyl)methanoneHCID 2213524214%

Reaction Steps

To a solution of bromoanisole 91 (1.38 mL, 10.7 mmol) in THF (5 mL) at 78° C. and under nitrogen atmosphere, was added 1.2 M t-BuLi in pentane (18.2 mL, 21.9 mmol) dropwise. After stirring for 20 min, anthranilonitrile 92 (0.63 g, 5.3 mmol) was added. The reaction was warmed to rt and stirred overnight. The reaction was cooled to 0° C. and quenched with 3N HCl. After stirring 30 min at rt, the acidic extracts were washed with EtOAc (3×12 mL). The aqueous layer was made basic (pH>10) using 6N NaOH and extracted with CH2Cl2. The organic extracts were washed with sat. NaCl, dried over NaSO4, filtered, and concentrated to give a crude mixture containing 93. The crude oil was purified by chromatography on silica to provide pure 93 (0.17 g, 14%) as a yellow oil; 1H NMR (500 MHz, DMSO-d6) δ 7.40–7.43 (m, 1H), 7.27–7.30 (m, 1H), 7.07–7.17 (m, 4H), 6.86–6.88 (m, 1H), 6.49–6.52 (m, 1H), 3.81 (s, 3H); CI MS m/z=228 [C14H13NO2+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053084B1
Source datasetuspto-grants-2006_05
ORD IDord-5c14dd280f9a452e821bc266bfcbaaa4
Source noteuspto-grants-2006_05