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HRID 1764840作成日:2026年10月27日

(2-Chloro-6-nitrophenyl)(3-chloropropyl)sulfane → 3-Chloro-2-[(3-chloropropyl)sulfanyl]aniline

https://huagongshe.com/reaction/1764840

反応式

関与物質

役割名称HCID仕込み量
反応物(2-Chloro-6-nitrophenyl)(3-chloropropyl)sulfaneHCID 22735865—
溶媒MethanolHCID 887—
生成物3-Chloro-2-[(3-chloropropyl)sulfanyl]anilineHCID 2273553793%

反応手順

The crude 1-chloro-2-[(3-chloropropyl)sulfanyl]-3-nitrobenzene was dissolved in MeOH (150 mL) and degassed with N2. Palladium hydroxide (1.8 g) was added in four portions to this solution in a Parr apparatus. The resulting heterogeneous solution was shaken under hydrogenation conditions (55 psi) at room temp for 18 h. The catalyst was removed via filtration in the same manner as above and the filtrate was concentrated in vacuo. to afford 3-chloro-2-[(3-chloropropyl)sulfanyl]aniline (9.94 g, 93%) as a dark oil: 1H NMR (CHCl3, 300 MHz) δ7.03 (t, 1H, J=8.1 Hz), 6.82 (t, 1H, J=8.1 Hz), 6.63 (t, 1H, J=8.0 Hz), 4.62 (br s, 1H), 3.68 (t, 2H, J=6.4 Hz), 2.92 (t, 2H, J=6.9 Hz), 1.98 (quintet, 2H, J=6.6 Hz) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE039679E1
出典データセットuspto-grants-2007_06
ORD IDord-bd277ece4407459a83ebc0648c74a3be
出典メモuspto-grants-2007_06