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HRID 1455038作成日:2026年10月27日

Thionyl Chloride → 6-Methoxy-2-phenylindan-1-one

https://huagongshe.com/reaction/1455038

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物3-(4-Methoxyphenyl)-2-phenylpropionic acidHCID 97739—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物6-Methoxy-2-phenylindan-1-oneHCID 2246537667.8%

反応条件

温度40 °C

反応手順

To solution of 3-(4-methoxyphenyl)-2-phenylpropionic acid (4.6 g) in dry methylene chloride (26 ml) was added two drops of dry DMF. Thionylchloride (3 ml) was added and reaction mixture was stirred at 40° C. for 4 h. Solvent was evaporated under vacuum. Precipitate was dissolved to methylene chloride. Solution was cooled to 0-3° C. This solution and aluminium chloride (2.5 g) were mixed slowly over 4 hours keeping temperature under 4° C. After mixing reaction mixture was stirred at room temperature for 2 h. Reaction was quenched by pouring to dilute ice cold hydrochloric acid. Layers were separated and water solution was extracted with methylene chloride. Combined organic layers were washed with water, dried and evaporated. Crude product was triturated to give 2.9 g of 6-Methoxy-2-phenylindan-1-one. 1H-NMR (400 MHz, d6-DMSO): 7.56 (d, 1H), 7.35-7.23 (m, 4H), 7.18-7.13 (m, 3H), 4.02 (dd, 1H, J 3.9, 8.0 Hz), 3.82 (s, 3H), 3.61 (dd, 1H, J 8.0, 17.2 Hz), 3.11 (dd, 1H, J 3.9, 17.2 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07482340B2
出典データセットuspto-grants-2009_01
ORD IDord-487dc2444aa6400380ad58a24716f521
出典メモuspto-grants-2009_01