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HRID 30890作成日:2026年10月25日

Sulfuryl chloride → 2-Chloro-5-(trifluoromethyl)-1,3-benzothiazole

https://huagongshe.com/reaction/30890

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuryl chlorideHCID 24648—
反応物5-(trifluoromethyl)-1,3-benzothiazole-2-thiolHCID 178419087—
生成物2-Chloro-5-(trifluoromethyl)-1,3-benzothiazoleHCID 2198584994%

反応手順

Sulfuryl chloride (9.09 g, 67.33 mmol) was added with stirring to 2-mercapto-5-(trifluoromethyl)benzothiazole (2.64 g, 11.22 mmol) over a period of 5 minutes. The reaction mixture was then allowed to stand for approximately 1 h. Ice water was added to the reaction mixture with stirring to decompose the excess of sulfuryl chloride, and the product was then extracted with ethyl acetate. The organic layer was washed with water (3×) and brine, dried over anhydrous Na2SO4 and concentrated. The resulting solid was dissolved in EtOAc and filtered though a short silica-gel column, eluting with EtOAc, to give 2-chloro-5-(trifluoromethyl)benzothiazole (2.50 g, 94%). LC-MS m/z 238.0 (MH+), ret. time 2.55 min; 1H NMR (400 MHz, DMSO-d6) δ 7.81 (d, 1H), 8.38 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423156B2
出典データセットuspto-grants-2008_09
ORD IDord-921fd12bd97a499788225f411c64e142
出典メモuspto-grants-2008_09