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HRID 50964作成日:2026年10月25日

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

https://huagongshe.com/reaction/50964

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 appararus. 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US06713471B1
出典データセットuspto-grants-2004_03
ORD IDord-904e74b753614e24915791cedb72e393
出典メモuspto-grants-2004_03