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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 659229생성일: 2026년 10월 25일

Acetic Acid → 4-(Trifluoromethyl)benzamide

https://huagongshe.com/reaction/659229

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PyrrolidineHCID 31268—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물2-methoxy-6-methylsulfanyl-N-(2-oxo-cyclohexyl)-4-trifluoromethyl-benzamideHCID 58062969—
용매TetrahydrofuranHCID 8028—
생성물4-(Trifluoromethyl)benzamideHCID 7468462.9%

반응 단계

2-Methoxy-6-methylsulfanyl-N-(2-oxo-cyclohexyl)-4-trifluoromethyl-benzamide (intermediate B, 380 mg, 1.05 mmol) was dissolved in 10 mL tetrahydrofurane. Acetic acid (145 mg, 2.4 mmol) and pyrrolidine (97 mg, 1.4 mmol) were added and the reaction mixture was stirred 1 h at room temperature. Sodium triacetoxyborohydride (290 mg, 1.4 mmol) was added and stirring was continued at room temperature overnight. The mixture was extracted with 2N sodium carbonate solution and ethyl acetate. The combined organic phases were dried on sodium sulfate, filtered and evaporated. Purification of the residue by flash chromatography on silica gel (dichloromethane/methanol/ammonia 100:0:0→140:10:1) yielded cis-2-methoxy-6-methylsulfanyl-N-2-pyrrolidin-1-yl-cyclohexyl)-4-trifluoromethyl-benzamide as a light yellow solid (125 mg, 28%), MS: m/e=417.3 [(M+H)+] and trans-2-methoxy-6-methylsulfanyl-N-2-pyrrolidin-1-yl-cyclohexyl)-4-trifluoromethyl-benzamide as a light yellow solid (28 mg, 6%), MS: m/e=417.3 [(M+H)+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08080541B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-d2e99e10e4a748b2982262634b7d0862
출처 메모uspto-grants-2011_12