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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51384Generated: October 27, 2026

Sodium Iodide → 9-[(3-trifluoromethylphenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-one

https://huagongshe.com/reaction/51384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant3-(Trifluoromethyl)benzyl chlorideHCID 69716—
Reactantmethyl 4-oxo-2,3,4,9-tetrahydro-1H-carbazole-5-carboxylateHCID 11368514—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product9-[(3-trifluoromethylphenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-oneHCID 2274051563.5%

Reaction Steps

40% Methanolic Triton B (2.18 mL, 4.8 mM) was slowly added dropwise to a solution of 5-carbomethoxy-1,2-dihydro-9H-carbazol-4(3H)-one (973 mg, 4.0 mM) in 10 mL of DMF at −10° C. After 30 minutes, 3-(trifluoromethyl)benzyl chloride (1.53 g, 6.0 mM) and sodium iodide (900 mg, 6.0 mM) were added and the resultant mixture stirred at room temperature for 25 hours. The mixture was diluted with ethyl acetate, washed five times with H2O, 1 N HCl, H2O, sat NaHCO3, and saturated brine, dried over anhydrous magnesium sulfate, filtered, concentrated, and dried in vacuo. The residue was purified by column chromatography on silica gel (elution with gradient methylene chloride/ethyl acetate) to afford 1.02 g (63%) of the 9-[(3-trifluoromethylphenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-one as a tan solid. 1H NMR (CDCl3) δ7.6 (d, 1H, J=8 Hz), 7.45-7.2 (m, 5H), 7.0 (d, 1H, J=8 Hz), 5.4 (s, 2H), 4.05 (s, 3H), 2.85 (t, 2H, J=6 Hz), 2.6 (t, 2H, J=6 Hz), and 2.2 (m, 2H). IR (KBr, cm−1) 1727 and 1652. MS (ES) m/e 400, 402.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713645B1
Source datasetuspto-grants-2004_03
ORD IDord-bc3a4330df02463a8bc84869761a8159
Source noteuspto-grants-2004_03