HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1632039Erstellt: 25. Oktober 2026
1,2-Dimethoxyethane → [4-(3-Bromo-4-methoxy-benzyl)-phenyl]-urea
https://huagongshe.com/reaction/1632039
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dimethoxyethane | HCID 8071 | — |
| Edukt | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Edukt | 2-Bromo-4-(bromomethyl)-1-methoxybenzene | HCID 11277462 | — |
| Edukt | 4-(Carbamoylamino)benzeneboronic acid, pinacol ester | HCID 16727440 | — |
| Katalysator | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | [4-(3-Bromo-4-methoxy-benzyl)-phenyl]-urea | HCID 57703725 | 36,9% |
Reaktionsschritte
To a 40 mL vial equipped with a teflon screw cap and a magnetic stir bar was added 2-bromo-4-bromomethyl-1-methoxybenzene (649 mg, 2.32 mmol), [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-urea (577 mg, 2.20 mmol) and potassium phosphate (933 mg, 4.40 mmol). To the vial was then added dimethoxyethane (15 mL), ethanol (3.7 mL) and water (3.7 mL). To this stirring solution was added tetrakis(triphenylphosphine) palladium (127 mg, 0.11 mmol) and the solution was degassed by bubbling N2 gas through the solution for 20 min. The vial was capped and placed in an oil bath with stirring at 65° C. for 12.5 h. The cooled reaction mixture was concentrated under a stream of N2 gas to a total volume of ˜5 mL and then diluted with ethyl acetate (20 mL) and water (10 mL). Upon shaking a white solid precipitates. The solid is filtered and dried to afford 272 mg (34%) of [4-(3-bromo-4-methoxy-benzyl)-phenyl]-urea (I-44) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08791267B2 |
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| Quelldatensatz | uspto-grants-2014_07 |
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| ORD ID | ord-6f485a0cb96a40f180a0a703e3c69b5c |
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| Quellennotiz | uspto-grants-2014_07 |
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