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HRID 374868作成日:2026年10月26日

Dimethylformamide → 6-Hydroxy-2-naphthaldehyde

https://huagongshe.com/reaction/374868

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物HexamethylphosphoramideHCID 12679—
反応物6-Bromo-2-naphthalenolHCID 27144—
反応物n-Butyl lithiumHCID 61028—
反応物HCID 178418306HCID 178418306—
溶媒TetrahydrofuranHCID 8028—
生成物6-Hydroxy-2-naphthaldehydeHCID 276411081%

反応手順

Step a) N-Butyllithium (35.9 mL, 89.7 mmol) was added dropwise to a cold (-78° C.) solution of 6-bromo-2-naphthol (20.0 g, 89.7 mmol) in THF (200 mL). After stirring for 10 minutes, tertbutyllithium (52.76 mL, 89.7 mmol) was added dropwise. The mixture was stirred for 30 min at -78° C, and two hours at -20° C. Then, hexamethylphosphoramide (15.6 mL, 89.7 mmol) was added to the reaction mixture. After stirring for 20 minutes. N,N-dimethylformamide (6.94 mL, 89.7 mmol) was added dropwise. The mixture was allowed to come to room temperature, stirred for 1 hour, and quenched with aqueous ammonium chloride. The mixture was poured into water, acidified with 2N HCL and extracted with EtOAc. The organic extracts were dried over MgSO4. Evaporation and purification by flash chromatography (hexane/EtOAc 3/1 ), gave a yellow solid (12.5 g, 81% yield, m.p. 173°-174 ° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05482968
出典データセットuspto-grants-1996_01
ORD IDord-45a5ead73b5d4e6f824c9900e697d11b
出典メモuspto-grants-1996_01