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HRID 333204作成日:2026年10月26日

p-Toluenesulfonic acid → 1,3-Bis-(4-fluorobenzoyl)benzene thiosemicarbazone

https://huagongshe.com/reaction/333204

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物1,3-Bis(4-fluorobenzoyl)benzeneHCID 688263—
反応物ThiosemicarbazideHCID 2723789—
溶媒MethanolHCID 887—
生成物1,3-Bis-(4-fluorobenzoyl)benzene thiosemicarbazoneHCID 7816525052%

反応手順

1,3-bis-(4-fluorobenzoyl)benzene 12 (0.347 g, 1.08 mmol) was dissolved in anhydrous methanol (50 mL). The solution was heated at reflux for 15 min, and thiosemicarbazide (0.049 g, 0.54 mmol) and a catalytic amount of p-toluenesulfonic acid were added. After 10 h at reflux, the resulting solution was concentrated under reduced pressure. Purification using flash chromatography (silica gel, hexanes:ethyl acetate, 70:30) afforded the desired 1,3-bis-(4-fluorobenzoyl)benzene thiosemicarbazone (0.11 g, 0.278 mmol, 52% yield) as a white solid; 1H NMR (500 MHz, CDCl3): δ 8.67 (s, 1H, NH), 7.97 (m, 1H, ArH), 7.90 (m, 1H, ArH), 7.83 (m, 1H, ArH), 7.75 (m, 1H, ArH), 7.68 (m, 1H, ArH), 7.500 (m, 2H, ArH), 7.39 (s, 1H, NH2), 7.31 (m, 2H, ArH), 7.22 (ddd, J=8.5 Hz, 5.0 Hz, 3.0 Hz, 1H, ArH), 7.16 (ddd, J=8.5 Hz, 5.0 Hz, 3.0 Hz, 1H, ArH), 7.06 (ddd, J=8.5 Hz, 5.0 Hz, 3.0 Hz, 1H, ArH), 6.36 (s, 1H, NH2); HRMS (ESI) calculated for C21H15F2N3OSH (M+H)+ 396.0970, found 394.0834; HPLC retention time 13.740, 13.966 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877967B2
出典データセットuspto-grants-2014_11
ORD IDord-a10ef0d2f36843fa8a487e2296d36f7f
出典メモuspto-grants-2014_11