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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 436536생성일: 2026년 10월 26일

Diethyl Ether → 3-Butylcyclohexanone

https://huagongshe.com/reaction/436536

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Acetyl chlorideHCID 6367—
반응물2-Cyclohexen-1-oneHCID 13594—
반응물ButyllithiumHCID 178418339—
용매HexaneHCID 8058—
생성물3-ButylcyclohexanoneHCID 566193—
생성물Cyclohexanone, 2-acetyl-3-butyl-HCID 11310101—

반응 단계

To 20 ml of anhydrous diethyl ether was added 1.9 g (10 mmol) of cuprous iodide, and at -78° C in an atmosphere of nitrogen, 12.8 ml (20 mmol) of a 15 % by weight hexane solution of n-butyllithium was added. The mixture was stirred for 30 minutes, and then, 960 mg (10 mmol) of 2-cyclohexenone was added. The mixture was further stirred for one hour. Then, 3.93 g (50 mmol) of acetyl chloride was added, and the mixture was stirred for 2 hours at room temperature. After the reaction, the reaction product was post-treated, extracted, washed, and dried in the same way as in Example 4 to afford 2.662 g of a crude product. The crude product was purified by column chromatography (silica gel) to afford 56 mg (0.4 mmol) of 3-n-butylcyclohexanone as a by-product in a yield of 4% and 1.103 g (5.6 mmol) of 2-acetyl-3-n-butylcyclohexanone as a main product in a yield of 56%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04009196
출처 데이터셋uspto-grants-1977_02
ORD IDord-8f8cebf8f8dd43fe8b942042a16aec72
출처 메모uspto-grants-1977_02