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HRID 30553作成日:2026年10月23日

Water → 1-{[4-(Difluoromethoxy)phenyl]ethynyl}-3-propylbenzene

https://huagongshe.com/ja/reaction/30553

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylboraneHCID 7357—
反応物Sodium HydroxideHCID 14798—
反応物N-[(E)-[3-[2-[4-(difluoromethoxy)phenyl]ethynyl]phenyl]methylideneamino]-4-methylbenzenesulfonamideHCID 59790336—
溶媒TetrahydrofuranHCID 8028—
生成物1-{[4-(Difluoromethoxy)phenyl]ethynyl}-3-propylbenzeneHCID 5743585689%

反応手順

A mixture of N′-[(1E)-(3-{[4-(difluoromethoxy)phenyl]ethynyl}phenyl)methylene]-4-methylbenzenesulfonohydrazide (0.67 mg, 1.52 mmol) in THF was treated with triethyl borane (1.0 M in THF, 1.52 mL, 1.52 mmol), stirred for 2 minutes, treated with NaOH (2.5 N, 0.61 mL, 1.52 mmol), refluxed for 2 hours, cooled to room temperature, poured into water and extracted with EtOAc. The organic extracts were combined, dried over MgSO4 and concentrated in vacuo. The resultant residue was purified on silica gel (ISCO) using hexanes/EtOAc (50/1) as the eluting solvents to give 1-{[4-(difluoromethoxy)phenyl]ethynyl}-3-propylbenzene as a clear oil (386 mg, 89% yield), MS m/e (M+H)+ 286; 1H NMR (400 MHz, DMSO-d6) 0.85 (t, J=7.32 Hz, 3H), 1.57 (m, 2H), 2.6 (t, J=7.32 Hz, 2H), 7.2 (m, 3H), 7.35-7.45 (m, 4H), 7.58 (d, J=8.79 Hz, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423158B2
出典データセットuspto-grants-2008_09
ORD IDord-2afa4f797d6842c69a7d8f1808c9d185
出典メモuspto-grants-2008_09