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HRID 30551作成日:2026年10月26日

Hydrochloric Acid → 3-{[4-(Difluoromethoxy)phenyl]ethynyl}benzaldehyde

https://huagongshe.com/reaction/30551

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TetrahydrofuranHCID 8028—
反応物2-(3-{[4-(Difluoromethoxy)phenyl]ethynyl}phenyl)-1,3-dioxolaneHCID 59790301—
溶媒WaterHCID 962—
生成物3-{[4-(Difluoromethoxy)phenyl]ethynyl}benzaldehydeHCID 57435855432.5%

反応手順

Into a mixture of 2-(3-{[4-(difluoromethoxy)phenyl]ethynyl}phenyl)-1,3-dioxolane, (1.0 g, 3.1 mmol) and THF (5 mL) was added HCl (2N, 1 mL). The mixture was stirred at room temperature for 2 hours, poured into water and extracted with EtOAc/ethyl ether 1/1. The organic extracts were dried over MgSO4. Evaporation and purification on silica gel (ISCO) using hexanes/EtOAc (3/1) as the eluting solvents gave 3-{[4-(difluoromethoxy)phenyl]ethynyl}benzaldehyde as a yellow oil (3.65 g, 95% yield), MS m/e M+ 272; 1H NMR (400 MHz, DMSO-d6) 3.9-4.05 (m, 4H), 5.72 (s, 1H), 7.1-7.3 (m, 4H), 7.62 (m, 2H), 7.8-7.9 (m, 2H), 8.03 (s, 1H), 9.99 (s, 1H).

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-6d9370bc6fab4c8ba5e07a254eae4b49
出典メモuspto-grants-2008_09