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HRID 18668作成日:2026年10月25日

Potassium Carbonate → 2-(4-Methoxy-2-propan-2-ylphenoxy)acetonitrile

https://huagongshe.com/reaction/18668

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Acetonitrile, 2-(((4-methylphenyl)sulfonyl)oxy)-HCID 84525—
反応物4-Methoxy-2-(propan-2-yl)phenolHCID 18364997—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物2-(4-Methoxy-2-propan-2-ylphenoxy)acetonitrileHCID 25241771—

反応手順

A stirred slurry of toluene-4-sulfonic acid cyanomethyl ester (13.0 kg), potassium carbonate (13.0 kg) and 2-isopropyl-4-methoxyphenol (9.57 Kg) in 79.7 kg of 2-butanone was heated to 55-60 degrees C. for 4 days, then heated to relux for 18 hours. The resultant slurry was cooled and filtered to remove solids. The filtrate was concentrated under reduced pressure and the residue was redissolved in toluene. The toluene solution was extracted with 1N KOH, and the organic phase was concentrated by distillation to give 20.6 g of a 1:1 (by weight) solution of (2-Isopropyl-4-methoxy-phenoxy)-acetonitrile in toluene, which was used directly in the next step. A anliquot (96.7 g) of this solution was concentrated to dryness to give 50.9 g of crude (2-Isopropyl-4-methoxy-phenoxy)-acetonitrile, projecting to a yield of 10.9 kg in the bulk solution: MS (M+H)=206; 1H nmr (CDCl3) delta: 1.25 (d, J=6.9 Hz), 3.31 (septet, 1H, J=6.9 Hz), 3.82 (s, 3H), 4.76 (s, 2H), 6.73 (dd. 1H, J=8.8 Hz, 3.1 Hz), 6.87 (d, 1H, J=3.1 Hz), 6.91 (d, 1H, J=8.8 Hz)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741484B2
出典データセットuspto-grants-2010_06
ORD IDord-cf9b8be9f1a34379a13bab8f30306493
出典メモuspto-grants-2010_06