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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22735649 | HCID 22735649 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Bromo-2-[(3-chloropropyl)sulfanyl]aniline | HCID 22735760 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039679E1 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-4eddc9ca713d4d24ac918ca5eaf51c2e |
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| Source note | uspto-grants-2007_06 |
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