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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 595079생성일: 2026년 10월 24일

Bromine → 2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one

https://huagongshe.com/ko/reaction/595079

반응식

참여 물질

역할이름HCID투입량
반응물BromineHCID 24408—
반응물DimedoneHCID 31358—
반응물Sodium AcetateHCID 517045—
반응물ThioureaHCID 2723790—
용매Acetic AcidHCID 176—
생성물2-Amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-oneHCID 58787475.2%

반응 단계

5,5-Dimethyl-cyclohexane-1,3-dione (201 g, 1.43 mol) and NaOAc (176 g, 2.14 mol) are suspended in AcOH (2 L) and Br2 (229 g, 1.43 mol) is added in dropwise while maintaining the reaction temperature between 15 and 20° C. After complete addition, the reaction is stirred at RT overnight. Thiourea (109 g, 1.43 mol) is added in portions and the reaction mixture is heated at 100° C. for 1 h. After cooling to RT, the AcOH is removed in vacuo and the resulting crude product is diluted with water (1 L) and neutralized with an aqueous saturated NaHCO3 solution. The resulting mixture is extracted with ethyl acetate (4×500 mL). The organic layer is washed with brine (500 mL), dried over anhydrous Na2SO4 and the solvent is evaporated in vacuo to give crude product. The crude product is washed with water (1.5 L) to yield 2-amino-5,5-dimethyl-5,6-dihydro-4H-benzothiazol-7-one (211 g, 75% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09243000B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-d4cdbd65aaa3462697dbdaa6824b1482
출처 메모uspto-grants-2016_01