戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 3714作成日:2026年10月24日

Benzenamine, 3,5-bis(trifluoromethyl)- → N-[3,5-bis(trifluoromethyl)phenyl]-2-[[2-[[3,5-bis(trifluoromethyl)phenyl]carbamoyl]phenyl]disulfanyl]benzamide

https://huagongshe.com/ja/reaction/3714

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenamine, 3,5-bis(trifluoromethyl)-HCID 9480—
反応物2,2'-Dithiodibenzoyl chlorideHCID 88164—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物N-[3,5-bis(trifluoromethyl)phenyl]-2-[[2-[[3,5-bis(trifluoromethyl)phenyl]carbamoyl]phenyl]disulfanyl]benzamideHCID 4653528%

反応手順

This compound was prepared according to the general method of Example 77 using 2,2'-dithiobisbenzoyl chloride (2.00 g, 5.83 mmol) in 50 mL of dichloromethane and 3,5-bis(trifluoromethyl)aniline (2.66 g, 11.6 mmol) in 21 mL of pyridine. The crude product was recrystallized from ethyl acetate-hexanes (1:9) to yield 0.34 g of the title compound, mp 213°-214° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05734081
出典データセットuspto-grants-1998_03
ORD IDord-4d69713b0abd4540ba7707592879c8e1
出典メモuspto-grants-1998_03