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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1650078생성일: 2026년 10월 27일

Hydrochloric Acid → 2-Mercapto-6-methylbenzoic acid

https://huagongshe.com/reaction/1650078

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium disulfideHCID 89870—
반응물Sodium NitriteHCID 23668193—
반응물2-Amino-6-methylbenzoic acid hydrochlorideHCID 70093546—
용매WaterHCID 962—
생성물2-Mercapto-6-methylbenzoic acidHCID 1261280980.3%

반응 단계

5.0 g of 2-amino-6-methylbenzoic acid hydrochloride was converted to a diazonium salt with concentrated hydrochloric acid and 2.3 g of sodium nitrite. Then, this diazonium salt was gradually dropwise added to a previously prepared sodium disulfide solution (which was prepared from 8.7 g of sodium sulfide nonahydrate, 1.1 g of sulfur, 1.5 g of sodium hydroxide and 15 ml of water) at from 0° to 5° C. After the completion of the dropwise addition, the mixture was stirred at room temperature for 2 hours to complete the reaction. The reaction solution was poured into a large amount of water, and concentrated hydrochloric acid was added thereto. Then, the mixture was extracted with ethyl acetate. A sodium hydrogen carbonate aqueous solution was added to the ethyl acetate layer, and sodium hydrogencarbonate-soluble components were extracted. 5.8 g of sodium pyrosulfate was added to the aqueous solution, and the mixture was refluxed for 30 minutes to complete the reaction. Concentrated hydrochloric acid was added to the reaction solution, and then the mixture was extracted with ethyl acetate. The extract was dried, and then the solvent was distilled off under reduced pressure to obtain 3.6 g (yield: 65%) of 2-mercapto-6-methylbenzoic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04923501
출처 데이터셋uspto-grants-1990_05
ORD IDord-7bcd31f5f7f94bb1989f66058337c07a
출처 메모uspto-grants-1990_05