HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 969481Erstellt: 24. Oktober 2026
Potassium Carbonate → Tert-butyl(4'-hydroxybiphenyl-3-ylmethyl)methylcarbamate
https://huagongshe.com/de/reaction/969481
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Hydroxyphenylboronic acid | HCID 2734360 | — |
| Edukt | tert-Butyl 3-bromobenzyl(methyl)carbamate | HCID 20738487 | — |
| Katalysator | HCID 178420554 | HCID 178420554 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,2-Dimethoxyethane | HCID 8071 | — |
| Produkt | Tert-butyl(4'-hydroxybiphenyl-3-ylmethyl)methylcarbamate | HCID 69643261 | 68% |
Reaktionsschritte
41.6 ml (83.2 mmol) of aqueous 2M potassium carbonate solution are added dropwise to a solution of 10 g (33 mmol) of tert-butyl (3-bromobenzyl)-N-methylcarbamate and 8.3 g (60 mmol) of 4-hydroxybenzeneboronic acid in 100 ml of ethylene glycol dimethyl ether. The reaction medium is degassed and 1.9 g (1.7 mmol) of tetrakis(triphenylphosphino)palladium are added. After heating for 12 hours at 80° C., the reaction medium is cooled, diluted with water and extracted with ethyl acetate. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 7 g of tert-butyl (4′-hydroxybiphenyl-3-ylmethyl)methylcarbamate are obtained in the form of a beige-colored solid, in a yield of 68%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07307078B2 |
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| Quelldatensatz | uspto-grants-2007_12 |
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| ORD ID | ord-1dfe92e2a34c44d4891e5ed515bff36e |
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| Quellennotiz | uspto-grants-2007_12 |
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