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HRID 51362作成日:2026年10月26日

Potassium Carbonate → 9-[(3-chlorophenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-one

https://huagongshe.com/reaction/51362

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
反応物methyl 4-oxo-2,3,4,9-tetrahydro-1H-carbazole-5-carboxylateHCID 11368514—
触媒Sodium IodideHCID 5238—
溶媒Ethyl AcetateHCID 8857—
生成物9-[(3-chlorophenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-oneHCID 2273858067.4%

反応手順

A suspension of 5-carbomethoxy-1,2-dihydro-9H-carbazol-4(3H)-one (527.0 mg, 2.17 mM), 3-chlorobenzyl bromide (802.2 mg, 3.90 mM), a catalytic amount of sodium iodide (ca. 1 mg), and potassium carbonate (500.0 mg, 3.62 mM) was stirred at room temperature for 150 hours. The mixture was diluted with ethyl acetate, washed five times with H2O, once with saturated brine, dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (elution with gradient methylene chloride/ethyl acetate) to afford 537.1 mg (67%) of the 9-[(3-chlorophenyl)methyl]-5-carbomethoxy-1,2-dihydrocarbazol-4(3H)-one as a yellow foam. 1H NMR (CDCl3) δ7.5-7.2 (m, 5H), 7.1 (s, 1H), 6.85 (m, 1H), 5.35 (s, 2H), 4.05 (s, 3H), 2.9 (t, 2H, J=6 Hz), 2.65 (t, 2H, J=6 Hz), and 2.3 (m, 2H). IR (CDCl3, cm−1) 3050, 2950, 1725, 1654, 1464, 1444, 1432, 1288 and 1120. MS (ES) m/e 366, 368, 370.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713645B1
出典データセットuspto-grants-2004_03
ORD IDord-7c0660bcd9ae4b89be25ff49f264854d
出典メモuspto-grants-2004_03