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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1247535생성일: 2026년 10월 25일

Hydrochloric Acid → N-Ethyl-2-hydroxybenzamide

https://huagongshe.com/reaction/1247535

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodoethaneHCID 6340—
반응물Sodium CarbonateHCID 10340—
반응물Sodium HydroxideHCID 14798—
반응물2H-1,3-Benzoxazine-2,4(3H)-dioneHCID 16258—
용매DimethylacetamideHCID 31374—
생성물N-Ethyl-2-hydroxybenzamideHCID 78354—

반응 조건

온도80 °C

반응 단계

Dimethylacetamide (50 ml) and carsalam (10.00 g, 0.0613 mol) were placed into a round bottom flask fitted with nitrogen purge, cold water condenser and a magnetic stir bar. Sodium carbonate (6.50 g, 0.0613 mol) and iodoethane (4.38 ml, 0.0548 mol) were added and heating of the reaction mixture was started. Heating at 80° C. continued for 16 hours at which point heating was discontinued and the reaction mixture was allowed to cool to room temperature. The reaction mixture was then filtered through a sintered glass funnel and the filtrate was collected. Water was added to this filtrate until a white solid precipitated. The solid was isolated by filtration and placed in an Erlenmeyer flask with 2N aqueous sodium hydroxide solution (200 ml). This mixture was heated at reflux for approximately 1 hour and then stirred overnight at room temperature. This mixture was acidified with 2N aqueous hydrochloric acid and a yellow oil was noted to separate out. The reaction mixture was extracted two times with 200 ml portions of ethyl acetate. The combined ethyl acetate layers were washed two times with 200 ml portions of deionized water, dried with sodium sulfate and concentrated under vacuum. N-ethylsalicylamide was recovered as a yellow oil which, after drying overnight under vacuum, was isolated in a yield of 7.93 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129274B1
출처 데이터셋uspto-grants-2006_10
ORD IDord-a977f736f9ee4c32b9cdb7e7f031ccee
출처 메모uspto-grants-2006_10