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HRID 490857作成日:2026年10月26日

2-Bromothiophene → HCID 86078978、化合物

https://huagongshe.com/reaction/490857

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromothiopheneHCID 13851—
反応物Pentafluorobenzoyl chlorideHCID 75256—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒Carbon DisulfideHCID 6348—
生成物HCID 86078978HCID 8607897833.3%

反応手順

To a mixture of perfluorobenzoyl chloride (2.51 g, 10.9 mmol) and 2-bromothiophene (1.86 g, 11.4 mmol) in carbon disulfide (80 mL), aluminum chloride (2.90 g, 21.8 mmol) was added in portions over 10 min with vigorous mechanical stirring. The reaction mixture turned red and was stirred for 2.5 h before being quenched with water (80 mL). The organics were then separated, the aqueous layer extracted with carbon disulfide (3×50 mL), and the combined organics washed with water (3×100 mL) and dried over MgSO4. After filtration, the organics were concentrated in vacuo and the chromatographed on a silica gel column (hexane:ether=9:1) to yield 1.23 g (32%) green crystals. mp 51-54° C.; 1H NMR (DMSO): δ 7.78 (d, 2H, 3J=3.6 Hz), 7.54 (d, 2H, 3J=4.4 Hz); 19F NMR (DMSO): δ −142.1 (m, 2H), −151.6 (m, 1H), −160.6 (m, 2H) Anal. Calcd for C11H2BrF5OS: C 37.00, H 0.56. Found: C 37.37, H 0.83; MS (EI): m/z (%) 355.8 (92) [M+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528176B2
出典データセットuspto-grants-2009_05
ORD IDord-3755f55c2b0f42b1aaa99adce2ebf18f
出典メモuspto-grants-2009_05