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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49489생성일: 2026년 10월 23일

Hydrochloric Acid → 6-(5-Hydroxy-pent-1-ynyl)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/49489

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Pentyn-1-olHCID 79346—
반응물6-Trifluoromethanesulfonyloxy-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 86587009—
촉매Copper iodideHCID 83717—
촉매HCID 178418397HCID 178418397—
용매PiperidineHCID 8082—
생성물6-(5-Hydroxy-pent-1-ynyl)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 6951484893.7%

반응 단계

To 850 mg (2.2 mmol) 6-Trifluoromethanesulfonyloxy-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester in 5 ml piperidine, 128.0 mg (0.1 mmol) tetrakis(triphenylphosphine)palladium followed by 21.0 mg (0.1 mmol) copper iodide were added. The solution was evaporated and flushed with argon prior to the addition of 210 μl (2.2 mmol) 4-pentynol at 80° C. over a period of 45 min. Further 0.2 ml (2.1 mmol) 4-pentynol were added and the solution was stirred for 2 h. The mixture was added to ice water, acidified with 2M HCl and extracted with ether. The combined organic phases were washed with water and dried over Na2SO4. Purification by column chromatography with CH2Cl2/MeOH 30:1 yielded 650 mg (92%) 6-(5-Hydroxy-pent-1-ynyl)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester as light brown oil, MS: 316 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706751B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-262821030e08427d9a479b72890ab542
출처 메모uspto-grants-2004_03