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HRID 1978246생성일: 2026년 10월 24일

Isopropanol → 1-Isopropoxycyclohexene

https://huagongshe.com/ko/reaction/1978246

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물CyclohexanoneHCID 7967—
반응물Propane, 2,2',2''-[methylidynetris(oxy)]tris-HCID 78191—
반응물Sodium bisulfate monohydrateHCID 23673662—
생성물1-IsopropoxycyclohexeneHCID 436613681.7%

반응 조건

온도60 °C

반응 단계

To a mixture at room temperature containing 196.32 grams (2 mol) of cyclohexanone, 390.4 grams (2.06 mol) of triisopropyl orthoformate and 12.00 grams of isopropanol (0.2 mol), was added 7.6 grams (0.055 mol) of sodium hydrogensulfate monohydrate. The reaction was exothermic and upon addition of the catalyst, the temperature of the reaction mixture rose to 35° C., and was heated and maintained at 60° C. for 1 hour. The progress of the reaction was monitored by GC until the cyclohexanone content dropped to less than 2%. The isopropanol and isopropyl formate were distilled off under reduced pressure until the reaction mixture's temperature reached a maximum of 100° C. The reaction mixture was cooled to room temperature and filtered to remove sodium hydrogensulfate monohydrate (recovered). The pH value of the filtrate was adjusted to about 7˜8 by adding 0.8 gram of potassium iso-propoxide. The mixture was then heated under reduced pressure to remove unreacted cyclohexanone. The product, 1-isopropoxy-1-cyclohexene was isolated by distillation as a clear liquid; the yield was 81.7% with a purity exceeding 98%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06235944B1
출처 데이터셋uspto-grants-2001_05
ORD IDord-d286ee6461874790a52c5b142e85ede8
출처 메모uspto-grants-2001_05