HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374868Generated: October 25, 2026
Dimethylformamide → 6-Hydroxy-2-naphthaldehyde
https://huagongshe.com/reaction/374868
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Reactant | n-Butyl lithium | HCID 61028 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Hydroxy-2-naphthaldehyde | HCID 2764110 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05482968 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-45a5ead73b5d4e6f824c9900e697d11b |
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| Source note | uspto-grants-1996_01 |
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