HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181921Generated: October 31, 2026
Pyridine → 4-tert-Butyl-2-nitrophenyl trifluoromethanesulfonate
https://huagongshe.com/reaction/1181921
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenol, 4-(1,1-dimethylethyl)-2-nitro- | HCID 18661 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-tert-Butyl-2-nitrophenyl trifluoromethanesulfonate | HCID 23109015 | 87% |
Reaction Steps
Triflic anhydride (4.14 mL, 24.6 mmol) was added dropwise to a solution of 4-tert-butyl-2-nitrophenol (4.00 g, 20.5 mmol) and pyridine (2.16 mL, 26.7 mmol) in methylene chloride (50 mL) at 0° C. The yellow solution was stirred 0.25 h at 0° C., poured onto saturated aqueous NaHCO3 and extracted with methylene chloride. The combined extracts were washed with saturated aqueous NaHCO3, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by filtration through a plug of silica-gel (methylene chloride) to provide trifluoro-methanesulfonic acid 4-tert-butyl-2-nitro-phenyl ester (5.82 g, 87%) as a pale yellow oil which was utilized without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07285545B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-d9804a7043f54951a63815cb7e49e5ae |
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| Source note | uspto-grants-2007_10 |
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