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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374868Generated: October 25, 2026

Dimethylformamide → 6-Hydroxy-2-naphthaldehyde

https://huagongshe.com/reaction/374868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHexamethylphosphoramideHCID 12679—
Reactant6-Bromo-2-naphthalenolHCID 27144—
Reactantn-Butyl lithiumHCID 61028—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product6-Hydroxy-2-naphthaldehydeHCID 276411081%

Reaction Steps

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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482968
Source datasetuspto-grants-1996_01
ORD IDord-45a5ead73b5d4e6f824c9900e697d11b
Source noteuspto-grants-1996_01