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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1769263생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → 2-Allyloxy-1-methylethyl 5-chloroquinolin-8-oxyacetate

https://huagongshe.com/reaction/1769263

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물3-Pyridinamine, N,N-dimethyl-HCID 123378—
반응물2-Propanol, 1-(2-propenyloxy)-HCID 542178—
반응물CloquintocetHCID 15257197—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-Allyloxy-1-methylethyl 5-chloroquinolin-8-oxyacetateHCID 1548412972.4%

반응 조건

온도0 °C

반응 단계

5.0 g (0.021 mol) of 5-chloroquinolin-8-oxyacetic acid and 2.44 g (0.021 mol) of 2-allyloxy-1-methylethanol are suspended in a mixture of 40 ml of methylene chloride and 40 ml of dimethylformamide and the suspension is cooled to 0° C. 4.78 g (0.023 mol) of dicyclohexylcarbodiimide, dissolved in 10 ml of methylene chloride, are added dropwise at this temperature, and 200 mg of 3-(N,N-dimethylamino)-pyridine are then added. The mixture is stirred at room temperature for 15 hours and the precipitate which has separated out is filtered off with suction and rinsed with 50 ml of methylene chloride. The filtrate is washed with 100 ml of 0.5 N HCl, with 100 ml of potassium bicarbonate solution and with 3 portions of in each case 50 ml of water. The organic phase is dried over magnesium sulfate and the solvent is stripped off in vacuo. The residue is recrystallized from n-heptane. 5.1 g (72.4% of theory) of 2-allyloxy-1-methylethyl 5-chloroquinolin-8-oxyacetate of melting point 59° C. are obtained in this manner.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05380852
출처 데이터셋uspto-grants-1995_01
ORD IDord-df1b135afad3466692a98882f3761cf4
출처 메모uspto-grants-1995_01