戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 377059作成日:2026年10月26日

1,2,3,4-Tetrachlorobenzene → [2,2-Bis(2,3,4,5-tetrachlorophenyl) ethyl]trichlorosilane

https://huagongshe.com/reaction/377059

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3,4-TetrachlorobenzeneHCID 12463—
反応物Silane, trichloro(1,2-dichloroethyl)-HCID 79093—
反応物Aluminum(III) ChlorideHCID 6451240—
生成物[2,2-Bis(2,3,4,5-tetrachlorophenyl) ethyl]trichlorosilaneHCID 53867974220.1%

反応手順

In the same apparatus and procedures as EXAMPLE 1 above, 43.18 g (200 mmol) of 1,2,3,4-tetrachlorobenzene and 1.07 g (8.0 mmol) of aluminum chloride were alkylated with 9.30 g (40.0 mmol) of (1,2-dichloroethyl)trichlorosilane for 10 min at 130° C. The aluminum chloride catalyst was quenched with POCl3 and then stirred for another 30 min to complete the deactivation. Freshly distilled hexane(100 ml) was added to the reaction mixture and insoluble solids in hexane were filtered from the organic soultion. After hexane was distilled, the reaction products were vacuum distilled to give 10.41 g of [2,2-bis(2,3,4,5-tetrachlorophenyl) ethyl]trichlorosilane (bp; 218-222° C./0.5 torr, yield; 44%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06022987
出典データセットuspto-grants-2000_02
ORD IDord-005acce036c24ac3af248b0103f6e476
出典メモuspto-grants-2000_02