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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 892356생성일: 2026년 10월 25일

Hydrochloric Acid → 2-Mercapto-6-acetylbenzoic acid

https://huagongshe.com/reaction/892356

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium disulfideHCID 89870—
반응물2-Acetyl-6-aminobenzoic acidHCID 19089401—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물2-Mercapto-6-acetylbenzoic acidHCID 1908939190.4%

반응 단계

10.2 g of 2-amino-6-acetylbenzoic acid was converted into a diazonium salt with a mixture of 14.2 ml of concentrated hydrochloric acid, 40 ml of water and 4.3 g of sodium nitrite, and the diazonium salt was gradually added dropwise at a temperature of 0° to 5° C. to a sodium disulfide aqueous solution (prepared from 14.3 g of sodium sulfide.9H2O, 1.9 g of sulfur, 4.6 g of sodium hydroxide and 30 ml of water). After adding dropwise, the reaction liquor was stirred for 2 hours at room temperature to complete the reaction. The reaction liquor was poured into a large amount of water, and after adding concentrated hydrochloric acid thereto, the product was extracted with ethyl acetate. To the ethyl acetate layer, was added sodium hydrogencarbonate aqueous solution, and the content soluble in sodium hydrogencarbonate was extracted. To the resultant aqueous solution, was added 14.8 g of sodium pyrosulfate, and the mixture was refluxed for 30 minutes to complete the reaction. To the reaction liquor, was added concentrated hydrochloric acid, and the product was extracted with ethyl acetate. The extracted liquor was dried, and the solvent was distilled off under reduced pressure to obtain 10.1 g of 2-mercapto-6-acetylbenzoic acid at a yield of 90%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05118339
출처 데이터셋uspto-grants-1992_06
ORD IDord-1097b3a3a26d472e845640667a1936d5
출처 메모uspto-grants-1992_06