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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 436539생성일: 2026년 10월 24일

Phthalic Anhydride → 3-Butylcyclohexanone

https://huagongshe.com/ko/reaction/436539

반응식

참여 물질

역할이름HCID투입량
반응물Phthalic AnhydrideHCID 6811—
반응물2-Cyclohexen-1-oneHCID 13594—
반응물TributylphosphineHCID 13831—
반응물Sodium HydroxideHCID 14798—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물3-ButylcyclohexanoneHCID 56619353%

반응 단계

To 30 ml of anhydrous diethyl ether were added 3.8 g (20 mmol) of cuprous iodide and 4.0 g (20 mmol) of tri-n-butylphosphine, and the mixture was stirred for about 1 hour at room temperature in an atmosphere of nitrogen and then cooled to -78° C. Then, 25.6 ml (40 mmol) of a 15 % by weight hexane solution of n-butyllithium was added, and the mixture was stirred for 30 minutes, and 1.92 g (20 mmol) of 2-cyclohexenone was added. The mixture was further stirred for 1 hour at -78° C. Then, 5 ml of hexamethylphosphoric tiramide was added, and the mixture was stirred for about 10 minutes. Phthalic anhydride (2.96 g, 20 mmol) was further added, and the mixture was stirred for 3 hours at room temperature. After the reaction, a solution of 4 g (100 mmol) of sodium hydroxide in 50 ml of water was added, and the mixture was stirred for about 1 hour. It was extracted with ether, washed, and dried to afford 6.22 g of a crude product. The crude product was distilled to afford 1.62 g (10.5 mmol) of 3-n-butylcyclohexanone in a yield of 53%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04009196
출처 데이터셋uspto-grants-1977_02
ORD IDord-02cc188640d848deaa2c2349341f38ee
출처 메모uspto-grants-1977_02