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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764847Generated: October 31, 2026

HCID 22735649, compound → 5-Bromo-2-[(3-chloropropyl)sulfanyl]aniline

https://huagongshe.com/reaction/1764847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22735649HCID 22735649—
SolventMethanolHCID 887—
Product5-Bromo-2-[(3-chloropropyl)sulfanyl]anilineHCID 2273576073%

Reaction Steps

4-Bromo-1-[(3-chloropropyl)sulfanyl]-2-nitrobenzene (1.97 g, 7.1 mmol) was dissolved in MeOH (25 mL). The reaction flask was evacuated with nitrogen, and Pd(OH)2 on carbon (400 mg) was added. The reaction flask was evacuated with nitrogen several time before being subjected to an atmosphere of H2 (50 psi). The flask was shaken on a parr apparatus for 72 hrs. The reaction was filtered over a bed of celite and the residue was washed with MeOH (5 mL). The supernatant was concentrated, and the crude, black residue was purified by column chromatography (50-20% hexanes-CH2Cl2), to afford 5-bromo-2-[(3-chloropropyl)sulfanyl]aniline (1.28 g, 73%) as a clear oil. 1H NMR (CDCl3, 300 Mhz) δ7.20 (d, 1H, 8.0 Hz), 6.88 (d, 1H, 2.0 Hz), 6.79 (dd, 1H, 2.0 Hz, 8.0 Hz), 4.41 (s, 2H), 3.64 (t, 2H, 6.6 Hz), 2.86 (t, 2H, 7.0 Hz), 1.94-1.99 (m, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039679E1
Source datasetuspto-grants-2007_06
ORD IDord-4eddc9ca713d4d24ac918ca5eaf51c2e
Source noteuspto-grants-2007_06