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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50964Generated: October 25, 2026

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

https://huagongshe.com/reaction/50964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Chloro-6-nitrophenyl)(3-chloropropyl)sulfaneHCID 22735865—
SolventMethanolHCID 887—
Product3-Chloro-2-[(3-chloropropyl)sulfanyl]anilineHCID 2273553793%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713471B1
Source datasetuspto-grants-2004_03
ORD IDord-904e74b753614e24915791cedb72e393
Source noteuspto-grants-2004_03