HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642256Generated: October 30, 2026
Potassium tert-butoxide → HCID 68428371, compound
https://huagongshe.com/reaction/642256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 68428757 | HCID 68428757 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68428371 | HCID 68428371 | 96% |
Reaction Steps
To a solution of 5-bromo-2-[(tert-butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-4-tert-butyl-1-(4-fluoro-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester (4.0 g, ˜6.28 mmol) in THF (15 mL) at −78° C. was added a solution of KOtBu in THF (9.42 mL, 9.42 mmol, 1 M); the reaction was stirred for 30 min at −78° C. and for 30 at room temperature. The reaction was subsequently quenched with saturated ammonium chloride aqueous solution, extracted with EtOAc, washed with water, and saturated NaCl aqueous solution, dried over anhydrous sodium sulfate, filtered, concentrated, to give an oil, the title product (3.24 g, crude), which was not further purified. The title product, 1H NMR (200 MHz, CDCl3): δ (ppm)=4.4-7.0 (m, 4H), 4.5-4.1 (m, 5H), 1.6-1.2 (m, 21H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696223B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-5263959b11e1488fa93f5b2ba2286f0e |
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| Source note | uspto-grants-2010_04 |
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