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HRID 1622159作成日:2026年10月26日

N-acetyl-N'-tert-butyl-5-formyl-6-methoxy-biphenyl-3,3'-disulfonamide → N-acetyl 5-formyl-6-hydroxy-biphenyl-3,3'-disulfonamide

https://huagongshe.com/reaction/1622159

反応式

関与物質

役割名称HCID仕込み量
反応物N-acetyl-N'-tert-butyl-5-formyl-6-methoxy-biphenyl-3,3'-disulfonamideHCID 86607706—
溶媒DichloromethaneHCID 6344—
生成物N-acetyl 5-formyl-6-hydroxy-biphenyl-3,3'-disulfonamideHCID 8660773788.4%

反応手順

N-acetyl-N′-tert-butyl-5-formyl-6-methoxy-biphenyl-3,3′-disulfonamide (100 mg, 0.21 mmol), prepared as in Reference 19, was dissolved in dichloromethane (10 mL). The solution was flushed with nitrogen for 5 minutes and then boron tribromide (1.0 mL, 1M solution in dichloromethane) was added. The mixture was stirred at room temperature for 1 hour and then concentrated under by evaporation under reduced pressure. The residue was partitioned between water and ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The residue was passed through a short silica plug with pure ethyl acetate to give N-acetyl 5-formyl-6-hydroxy-biphenyl-3,3′-disulfonamide (74 mg) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08778625B2
出典データセットuspto-grants-2014_07
ORD IDord-68ed2e6906b0475797b1b7b88b7c15f3
出典メモuspto-grants-2014_07