HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383263Generated: November 1, 2026
4-Bromo-2-nitrophenol → 2-Amino-4-Bromophenol
https://huagongshe.com/reaction/383263
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromo-2-nitrophenol | HCID 24364 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-4-Bromophenol | HCID 351840 | 89.2% |
Reaction Steps
A mixture of compound 4-bromo-2-nitrophenol (1 g, 4.59 mmol) and SnCl2 (5.2 g, 22.9 mmol) in ethanol (10 mL) was stirred at 70° C. for 2 h. After cooled down, the mixture was diluted with water (100 mL), adjusted to pH 7 with saturated aqueous NaHCO3 and extracted with ethyl acetate (100 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4, concentrated to give 2-amino-4-bromophenol (770 mg, 89%) as a grey solid. LCMS: 188 [M+1]+. 1H NMR (400 MHz, DMSO-d6) δ 4.79 (s, 2H), 6.48 (dd, J1=2.4 Hz, J2=8.4 Hz, 1H), 6.55 (d, J=8.4 Hz, 1H), 6.71 (d, J=2.4 Hz, 1H), 9.26 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367663B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-c38e6cc82a00442093a2e29ec3a8a771 |
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| Source note | uspto-grants-2013_02 |
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