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HRID 472786作成日:2026年10月27日

Dimethylformamide → Methyl 6-formyl-1-naphthoate

https://huagongshe.com/reaction/472786

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物Trioctylsilane, 95%HCID 87780—
反応物Methyl 6-(((trifluoromethyl)sulfonyl)oxy)-1-naphthoateHCID 22622428—
反応物HCID 178418416HCID 178418416—
触媒palladium(II) acetateHCID 167845—
生成物Methyl 6-formyl-1-naphthoateHCID 5805697936%

反応条件

温度70 °C

反応手順

Carbon monoxide (CO) gas was slowly bubbled through a solution of methyl 6-(((trifluoromethyl)sulfonyl)oxy)-1-naphthoate (334 mg, 1.0 mmol), Pd(OAc)2 (22 mg, 0.10 mmol), 1,3-bis-(diphenylphosphino)propane (40 mg, 0.10 mmol) and triethylamine (0.28 mL, 2.0 mmol) an DMF (8.3 mL). After 15 min, trioctylsilane (0.90 mL, 2.0 mmol) was added as bubbling continued. The mixture was heated at 70° C., continuing to bubble CO into the solution. After 6 h at 70 the bubbling CO was replaced with a balloon of CO and the reaction mixture was stirred overnight. After 18 h at 70° C., the reaction was cooled to room temperature, diluted with EtOAc (150 mL) and washed with water (3×50 mL) and brine (50 mL). The organic phase was dried (Na2SO4), filtered and concentrated in vacuo. The resulting residue was purified on 40 g silica gel (100% hexanes→25% EtOAc/hexanes, gradient) to afford 78 mg (36%) of methyl 6-formyl-1-naphthoate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633220B2
出典データセットuspto-grants-2014_01
ORD IDord-f1f9697f468c45b4bb16255818f39e02
出典メモuspto-grants-2014_01