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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374868Erstellt: 24. Oktober 2026

Dimethylformamide → 6-Hydroxy-2-naphthaldehyde

https://huagongshe.com/de/reaction/374868

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktHexamethylphosphoramideHCID 12679—
Edukt6-Bromo-2-naphthalenolHCID 27144—
Eduktn-Butyl lithiumHCID 61028—
EduktHCID 178418306HCID 178418306—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-Hydroxy-2-naphthaldehydeHCID 276411081%

Reaktionsschritte

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.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05482968
Quelldatensatzuspto-grants-1996_01
ORD IDord-45a5ead73b5d4e6f824c9900e697d11b
Quellennotizuspto-grants-1996_01