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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 372429생성일: 2026년 10월 26일

Hydrochloric Acid → 2-Iodo-4-methoxybenzoic acid

https://huagongshe.com/reaction/372429

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sulfuric AcidHCID 1118—
반응물Potassium IodideHCID 4875—
반응물2-Amino-4-methoxybenzoic acidHCID 351010—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물2-Iodo-4-methoxybenzoic acidHCID 12822182—

반응 단계

150 G. of 4-methoxy-anthranilic acid are suspended in 1 liters of water and 80 ml. of concentrated hydrochloric acid at 0° C. To this suspension is added dropwise over a period of 30 minutes, with stirring at 0°-5° C, a solution of 62 g. of sodium nitrite in 130 ml. of water. The resulting diazonium salt solution is stirred for an additional 15 minutes at 0°-5° C. A solution of 164 g. of potassium iodide in 700 ml. of 5-N sulfuric acid is subsequently added dropwise at 3°-6° C. over a period of 45 minutes. The mixture is stirred at room temperature for 30 minutes and subsequently slowly heated to reflux. After boiling for 2 hours at reflux, the mixture is cooled to room temperature. The separated brown crystals are removed by filtration and washed neutral with water. The filter cake is dried under reduced pressure and there is obtained 2-iodo- 4-methoxy-benzoic acid as brown crystals which melt at 174° C. Then, the 2-iodo-4-methoxy-benzoic acid is converted in the manner described in Example 1 to give the desired starting material, 1-[10,11-dihydro-3-methoxy-8-methyl-dibenz[b,f]oxepin-10-yl]-piperazine, in the form of an oil. The following intermediates are obtained:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04091023
출처 데이터셋uspto-grants-1978_05
ORD IDord-6bcee9682d36408895a5f259d7721d35
출처 메모uspto-grants-1978_05