HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056106Generated: November 2, 2026
Sodium Thiosulfate → 2-Amino-4-(trifluoromethoxy)phenol
https://huagongshe.com/reaction/2056106
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 2-Nitro-4-(trifluoromethoxy)phenol | HCID 2775775 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-4-(trifluoromethoxy)phenol | HCID 2737729 | 56.2% |
Reaction Steps
To a mixture of 2-nitro-4-(trifluoromethoxy)phenol (2 g, 0.0089 mol) in ethanol (50 mL) and water (25 mL) was added sodium thiosulfate (6.2 g, 0.0356 mol) at room temperature. The heterogeneous mixture was stirred at 80° C. under an atmosphere of nitrogen for 1 hour. The reaction mixture was cooled to room temperature, and ethanol was removed under reduced pressure. The aqueous layer was extracted with ethyl acetate (3×70 mL), and the organic layer was washed with brine and dried under sodium sulfate. The solvent was removed under reduced pressure to give yellow solid of 2-amino-4-(trifluoromethoxy)phenol (0.9 g, 0.005 mol). TLC (methanol/dichloromethane=5:95) Rf 0.29 MS: MH+: 194
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07332497B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-396109b6c4e849f59544872c39ac9450 |
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| Source note | uspto-grants-2008_02 |
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