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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374868생성일: 2026년 10월 25일

Dimethylformamide → 6-Hydroxy-2-naphthaldehyde

https://huagongshe.com/reaction/374868

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물HexamethylphosphoramideHCID 12679—
반응물6-Bromo-2-naphthalenolHCID 27144—
반응물n-Butyl lithiumHCID 61028—
반응물HCID 178418306HCID 178418306—
용매TetrahydrofuranHCID 8028—
생성물6-Hydroxy-2-naphthaldehydeHCID 276411081%

반응 단계

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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05482968
출처 데이터셋uspto-grants-1996_01
ORD IDord-45a5ead73b5d4e6f824c9900e697d11b
출처 메모uspto-grants-1996_01