돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27466생성일: 2026년 10월 23일

Hydrogen Bromide → Benzoic Acid

https://huagongshe.com/ko/reaction/27466

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물Salicylic AcidHCID 338—
반응물Allyl bromideHCID 7841—
반응물Ethyl SalicylateHCID 8365—
반응물Sodium hydrideHCID 24758—
반응물Ethanol hydrochlorideHCID 21887872—
용매DimethylformamideHCID 6228—
생성물Benzoic AcidHCID 243—

반응 단계

13.6 g of 4-(2-<5-chloro-2-methoxy-benzamido>-ethyl)-2-hydroxy-benzoic acid ethyl ester, M.p. 88°-89° C., (prepared by treatment of 4-(2-aminoethyl)-2-methoxy-benzoic acid. HCl with hydrobromic acid/glacial acetic acid, reaction of the resulting 4-(2-<5-chloro-2-methoxy-benzamido>-ethyl)-2-hydroxy-benzoic acid with ethanol/HCl) were dissolved in 75 ml of DMF and combined with 1.2 g of sodium hydride/80% strength in white oil. The whole was stirred for half an hour, 4.4 g of allyl bromide were added and stirring was continued for 4 hours at 65° C. The dimethylformamide was then eliminated by distillation under reduced pressure, the residue was dissolved in ether, washed with sodium hydroxide solution and water, the ether solution was concentrated by evaporation and the residue was hydrolyzed by heating with 100 ml of 10% sodium hydroxide solution in the presence of a small amount of ethanol. After cooling, the solution was acidified, the substance that had precipitated was re-precipitated from ammonia with the aid of charcoal and then crystallized from dilute methanol. The 2-allyloxy-4-(2-<5-chloro-2-methoxy-benzamido>-ethyl)-benzoic acid so obtained was found to melt at 122°-123° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04221815
출처 데이터셋uspto-grants-1980_09
ORD IDord-33c62ca187fe495582433e380d245f61
출처 메모uspto-grants-1980_09