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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371964생성일: 2026년 10월 24일

Ammonia → Cyclohexanone, trimethyl-

https://huagongshe.com/ko/reaction/371964

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물WaterHCID 962—
반응물1,4-Dichloro-2-buteneHCID 15122—
반응물2,2,6-TrimethylcyclohexanoneHCID 17000—
용매TetrahydrofuranHCID 8028—
생성물Cyclohexanone, trimethyl-HCID 301657019.6%

반응 단계

28 g of 2,2,6-trimethyl-cyclohexanone are added dropwise to a suspension of Na vinylacetylide (prepared from 25 g of 1,4-dichlorobut-2-ene and 15 g of Na in liquid ammonia) in 200 ml of THF, whilst cooling, and the reaction mixture is stirred overnight at room temperature. 50 ml of water are then added, the aqueous phase is extracted with ether and the resulting organic phase is dried and concentrated. Subsequent fractional distillation gives 5.5 g of unconverted trimethylcyclohexanone and 20.7 g (corresponding to 68% of theory, based on ketone converted) of 2,2,6-trimethyl-1-(but-1'-yn-3'-en-1'-yl)-cyclohexanol of boiling point 62°-63° C/0.3 mm Hg and refractive index nD25 = 1.4982. Fragrance note: fresh, tart-woody, coniferous.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04088681
출처 데이터셋uspto-grants-1978_05
ORD IDord-9a4f5dd4dae64917b167c5c127b60dfe
출처 메모uspto-grants-1978_05