戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1396作成日:2026年10月23日

Water → Methyl 5,5-dimethyl-5,6-dihydro-8-(phenylthio)-naphthalene-2-carboxylate

https://huagongshe.com/ja/reaction/1396

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物ThiophenolHCID 7969—
反応物TriethylamineHCID 8471—
反応物Methyl 5,5-dimethyl-5,6 dihydro-naphthalen-8(7h)-one-2-carboxylateHCID 10681077—
触媒Titanium TetrachlorideHCID 24193—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 5,5-dimethyl-5,6-dihydro-8-(phenylthio)-naphthalene-2-carboxylateHCID 22571588—

反応手順

To a solution of methyl-5,5-dimethyl-5,6-dihydro-naphthalen-8(7H)-one-2-carboxylate (Compound E2, 835.0 mg, 3.60 mmol) in 25.0 mL of THF at room temperature was added TiCl4 (670.0 mg, 3.55 mmol). Thereafter a solution of thiophenol (430.0 mg, 3.90 mmol) and Et3N (730.0 mg, 7.20 mmol) in 10 mL THF was added. The resulting brown mixture was stirred for 6 h before H2O was carefully added to quench the reaction. The product was extracted into Et2O and the combined organic layers washed with saturated aqueous NaCl and dried over MgSO4. Removal of the solvents under reduced pressure afforded a solid from which the title compound was isolated as a yellow solid by column chromatography (5% EtOAc-hexanes).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723666
出典データセットuspto-grants-1998_03
ORD IDord-83bf3c1c076c4485b404b1a77f65cfe6
出典メモuspto-grants-1998_03