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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2408248생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2408248

반응식

참여 물질

역할이름HCID투입량
반응물Phosphoric AcidHCID 1004—
반응물Allyl chlorideHCID 7850—
반응물2-Methyl-1-(4-methylphenyl)prop-2-en-1-olHCID 54023324—
촉매Tetrabutylammonium IodideHCID 67553—
용매TetrahydrofuranHCID 8028—
용매tert-Butyl methyl etherHCID 15413—
생성물1-[1-(Allyloxy)-2-methyl-2-propenyl]-4-methylbenzeneHCID 6733042180.2%

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08815792B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-563d9c62427f4feea5896d68521d16c0
출처 메모uspto-grants-2014_08