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HRID 19954作成日:2026年10月24日

Vanillin → 4-(N,N-Dimethylsulfamoyl)-3-methoxybenzaldehyde

https://huagongshe.com/ja/reaction/19954

反応式

関与物質

役割名称HCID仕込み量
反応物VanillinHCID 1183—
反応物Dimethylsulphamoyl chlorideHCID 83372—
反応物Ethyl acetate hexaneHCID 21226206—
溶媒N,N-DimethylcyclohexylamineHCID 7415—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物4-(N,N-Dimethylsulfamoyl)-3-methoxybenzaldehydeHCID 21976871—

反応手順

To a solution of vanillin (4.56 g, 30 mmol) in N,N-dimethylcyclohexylamine (30 mL) at 80-90° C., was added N,N-dimethylsulfamoyl chloride (3.79 mL, 35.27 mmol). The mixture was stirred at this temperature for 4 h, transferred to a separating funnel and diluted with EtOAc (100 mL). The organic layer was washed with water (2×200 mL), 6M HCl (aq.) (200 mL), brine (2×200 mL), dried (Na2SO4) and filtered. Concentration in vacuo of the combined filtrates gave a golden-yellow oil which solidified on standing. The product was stirred in n-hexane, filtered and air-dried to give OBS02011 as yellow plates (6.92 g, 89%). TLC [SiO2, EtOAc-n-hexane (1:1)] Rf=0.65; 1H-NMR (270 MHz, CDCl3)=2.98 (6H, s), 3.93 (3H, s), 7.44 (1H, d, J=1.6), 7.48 (1H, dd, J=1.6, 8.1), 7.53 (1H, d, J=8.1), 9.92 (1H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745472B2
出典データセットuspto-grants-2010_06
ORD IDord-c05a971138724dfeb0aba79d83b73319
出典メモuspto-grants-2010_06