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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1770106생성일: 2026년 10월 26일

Acetic Acid → Ethyl 2,4-dichloro-5-fluorobenzoylacetate

https://huagongshe.com/reaction/1770106

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물Acetophenone, 2',4'-dichloro-5'-fluoro-HCID 727250—
용매Diethyl CarbonateHCID 7766—
생성물Ethyl 2,4-dichloro-5-fluorobenzoylacetateHCID 2774350—

반응 단계

A 250 ml flame dried round bottom flask is equipped with a pressure equalizing addition funnel, magnetic stirring bar, and gas inlet. The flask is charged with a 50% sodium hydride-in-oil suspension (3.74 g, 78.0 mmol) along with 20 ml of dry THF. The slurry of NaH is cooled to 0° C. with an ice bath and a solution of 2,4-dichloro-5-fluoroacetophenone (7.8 g, 37.6 mmol) in 100 ml of diethylcarbonate (100 ml) is added slowly (dropwise) to the slurry of NaH. After the addition is complete the mixture is stirred at room temperature until gas evolution ceases (30 minutes). The deep red-orange solution is then heated to 80° C. for 1.5 hours. The reaction mixture is poured into an ice-cold water (250 ml) solution containing acetic acid (8 ml). The mixture is extracted (3×150 ml) with ether, dried over Na2SO4, and concentrated to an orange oil. The oil is distilled at high vacuum (1 mmHg 133°-135° C.). 7.9 g of ethyl 2,4-dichloro-5-fluorobenzoylacetate is obtained as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05385906
출처 데이터셋uspto-grants-1995_01
ORD IDord-07f9ee01bac1497e81bf17f656cf8874
출처 메모uspto-grants-1995_01