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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242152생성일: 2026년 10월 25일

Ethyl Acetate → (6-Chloropyridazin-3-yl)methanol

https://huagongshe.com/reaction/242152

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Thionyl ChlorideHCID 24386—
반응물Sodium borohydrideHCID 4311764—
반응물6-chloropyridazine-3-carboxylic AcidHCID 6415762—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물(6-Chloropyridazin-3-yl)methanolHCID 20557609—

반응 조건

온도60 °C

반응 단계

4.3 g (21.4 mmol) of 6-chloropyridazine-3-carboxylic acid are dissolved in 60 ml of dry toluene and heated to 60° C. At this temperature, 3.8 g (32.2 mmol) of thionyl chloride are added, and the mixture is stirred at this temperature for 3 h. The mixture is then heated at reflux for 4 h. After cooling to RT, the solvent is removed on a rotary evaporator. 20 ml of toluene are added, and the mixture is again evaporated to dryness. The residue is dissolved in 40 ml of methyl tert-butyl ether and cooled to 5° C. At this temperature, a solution of 1.7 g (47.2 mmol) of sodium borohydride in 37 ml of water is added dropwise. The mixture is stirred at RT for 20 h. 50 ml of ethyl acetate are then added, and the aqueous phase is extracted three times with in each case 10 ml of ethyl acetate. The combined organic phases are washed in each case twice with in each case 10 ml of sat. sodium bicarbonate solution and water. The solvent is removed on a rotary evaporator and the residue is purified chromatographically on silica gel 60 (mobile phase: gradient dichloromethane/ethanol 100:1→20:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653109B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-3fd82016978b4fd29e041774b9703100
출처 메모uspto-grants-2014_02