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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 372474생성일: 2026년 10월 26일

Pyridine → 4-Methylocta-4-ene-1,7-diyne-3-yl alpha-isopropyl-4-chlorophenylacetate

https://huagongshe.com/reaction/372474

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2-(4-Chlorophenyl)-3-methylbutanoyl chlorideHCID 4178001—
반응물4-Methylocta-4-ene-1,7-diyne-3-olHCID 54236197—
용매BenzeneHCID 241—
생성물4-Methylocta-4-ene-1,7-diyne-3-yl alpha-isopropyl-4-chlorophenylacetateHCID 5423199685.1%

반응 단계

1.40 Grams (11.4 millimoles) of 4-methylocta-4-ene-1,7-diyne-3-ol is dissolved in 20 ml of a dry benzene, followed by cooling in ice water. Thereafter, 1.80 g (22.8 millimoles) of pyridine is rapidly added thereto at a time and immediately a solution of 2.64 g (11.4 millimoles) of α-isopropyl-4-chlorophenylacetyl chloride in 10 ml of dry benzene is dropwise added thereto for about 30 minutes with stirring. After completion of the addition, stirring is continued for 3 hours at room temperature to complete the reaction. The reaction mixture is poured into 20 g of ice water and the layers are separated. The aqueous layer is extracted with two 10-ml portions of ether. The organic layers obtained is combined and washed once with a 10% hydrochloric acid and three times with water, followed by drying over anhydrous sodium sulfate. After the solvent is removed under reduced pressure, the oily substance obtained is mixed with almost the same amount of pyridine. The mixture is adsorbed to 100 g of silica gel column and purified by developing with a mixed solvent (18 : 1 : 1) of carbon tetrachloride : n-hexane : ether. Thus, 3.19 g of the objective ester is obtained as a pale yellow oily substance (85.1% of theoretical yield). nD23.0 1.5233

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04091111
출처 데이터셋uspto-grants-1978_05
ORD IDord-e75b1ebc56484f50a4c8b2da4711173d
출처 메모uspto-grants-1978_05