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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50971Generated: October 29, 2026

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

https://huagongshe.com/reaction/50971

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 supernant was concentrated, and the crude, balck 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 numberUS06713471B1
Source datasetuspto-grants-2004_03
ORD IDord-9de867f0fe5a4143af43a955f851091f
Source noteuspto-grants-2004_03