HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095828Generated: October 31, 2026
Potassium tert-butoxide → HCID 58158560, compound
https://huagongshe.com/reaction/2095828
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 58158465 | HCID 58158465 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58158560 | HCID 58158560 | 39% |
Reaction Steps
To a solution of 1-(3-bromobutyl)-3-(4-fluorophenyl)urea (1750 mg, 6.1 mmol) in N,N-dimethylformamide (30 mL) was added potassium tert-butoxide (920 mg, 7.0 mmol), and the mixture was stirred at 50° C. for 6 hr. The solvent was evaporated under reduced pressure, and ethyl acetate/tetrahydrofuran and 6N aqueous hydrochloric acid solution were added to the residue. The aqueous layer was extracted with ethyl acetate/tetrahydrofuran (×3). The combined organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH silica gel, ethyl acetate/hexane=50/50→100/0) to give the title compound (490 mg, 39%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445509B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-2feaca9eab3f40b29623361b67685c8d |
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| Source note | uspto-grants-2013_05 |
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