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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992829Generated: October 28, 2026

Sodium hydride → HCID 86616639, compound

https://huagongshe.com/reaction/1992829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Fluoro-2-(trifluoromethyl)benzaldehydeHCID 522940—
Reactant6-Methoxy-3-methyl-2-phenyl-1-naphtholHCID 68536388—
SolventDimethylformamideHCID 6228—
ProductHCID 86616639HCID 8661663990%

Reaction Conditions

Temperature0 °C

Reaction Steps

Compound 7 (215 mg, 0.81 mmol, 1 equiv) was dissolved in DMF (5 mL) and cooled to 0° C. under N2. Sodium hydride, 60% dispersion (36 mg, 0.89 mmol, 1.1 equiv), followed by 4-fluoro-2-(trifluoromethyl)benzaldehyde (312 mg, 1.63 mmol, 2 equiv) were added and the entire reaction mixture was heated to 70° C. for 3 days. The mixture was then partitioned between EtOAc (50 mL) and H2O (50 mL). The organic layer was washed with saturated aqueous NaCl (100 mL), dried over Na2SO4, filtered and concentrated to dryness. The residue was purified by silica gel flash column chomatography (10% EtOAc in hexanes) to provide 20 (308 mg, 87%) as a clear oil. 1HNMR (400 MHz, DMSO-d6): δ 10.01 (s, 1H), 7.89 (d, J=8.8 Hz, 1H), 7.78 (s, 1H), 7.60 (d, J=9.1 Hz, 1H), 7.39 (d, J=2.4 Hz, 1H), 7.32-7.10 (m, 7H), 6.95 (dd, J=8.6, 2.4 Hz, 1H), 3.88 (s, 3H), 2.20 (s, 3H). MS m/z 473.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649093B2
Source datasetuspto-grants-2010_01
ORD IDord-958795c2b1374783bec9c4b14a3fdbe0
Source noteuspto-grants-2010_01