戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2408248作成日:2026年10月27日

Phosphoric Acid → 1-[1-(Allyloxy)-2-methyl-2-propenyl]-4-methylbenzene

https://huagongshe.com/reaction/2408248

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphoric AcidHCID 1004—
反応物Allyl chlorideHCID 7850—
反応物2-Methyl-1-(4-methylphenyl)prop-2-en-1-olHCID 54023324—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒TetrahydrofuranHCID 8028—
溶媒tert-Butyl methyl etherHCID 15413—
生成物1-[1-(Allyloxy)-2-methyl-2-propenyl]-4-methylbenzeneHCID 6733042180.2%

反応手順

Solid sodium tert-butylate (66.65 g, 0.589 mol) was dissolved under nitrogen in dry THF (350 ml) and 1-(4-methylphenyl)-2-methyl-2-propen-1-ol (41.16 g, 0.239 mol) in dry THF (25 ml) was added in 15 minutes without external cooling. The reaction was further stirred at room temperature for 50 minutes. Tetra butyl ammonium iodide (5.04 g, 0.014 mol) was added followed by allyl chloride (40 g, 0.518 mol) in 25 minutes (exothermic to 47° C.). The reaction was stirred for 24 hours, before adding more tetra butyl ammonium iodide (2.30 g, 0.006 mol) and allyl chloride (9.30 g, 0.120 mol). After stirring for 24 hours at room temperature, the reaction was poured onto ice, diluted with MTBE and acidified with aqueous phosphoric acid. The organic phase was washed with brine, saturated aqueous sodium bicarbonate and brine and dried over solid anhydrous sodium sulfate. The solid was filtered off, rinsed with MTBE and solvents were removed under vacuum. The product was purified by distillation through a 35-cm Fisher column. 38.78 g of the desired allyl ether were obtained (yield=80%). B.P.=79° C./1.6 mbar

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08815792B2
出典データセットuspto-grants-2014_08
ORD IDord-563d9c62427f4feea5896d68521d16c0
出典メモuspto-grants-2014_08