HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634935Generated: October 25, 2026
2,3,5,6-Tetrafluorophenol → tert-Butyl pentanoate
https://huagongshe.com/reaction/634935
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3,5,6-Tetrafluorophenol | HCID 69858 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl ester | HCID 86756359 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl pentanoate | HCID 520048 | 371.5% |
| Product | N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl Ester | HCID 86756358 | — |
Reaction Steps
Potassium fluoride (21.6 mg, 0.37 mmol) was added to a solution of N-[(1-methyl-3-isobutyl-indole-2-carbonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl ester (86.1 mg, 0.149 mmol) and 2,3,5, 6-tetrafluorophenol (27.0 mg, 0.163 mmol) in DMF (2.0 ml). After stirring at room temperature for 3 hours, the reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was back-extracted with ethyl acetate. The organic layers were combined, washed with saturated NaHCO3 solution, and brine, dried over sodium sulfate, and concentrated. The residue was triturated with ether to give the titled product, N-(1-methyl-3-isobutyl-indole-2-carbonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetral]uorophenyloxy)-pentanoic acid, tert-butyl ester as a white solid (43.8 mg, 44%). TLC (hexane/EtOAc, 50/50): Rf=0.50.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06184244B2 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-6da38b4177ff47fe80c51126986009bb |
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| Source note | uspto-grants-2001_02 |
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