HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Lithium Hydroxide → (1R,2R)-2-(4-bromophenyl)Cyclopropanecarboxylic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Lithium Hydroxide | HCID 3939 | — |
| Edukt | 4-Bromostyrene | HCID 16263 | — |
| Edukt | Diazoacetate | HCID 21863207 | — |
| Edukt | ethyl (1R,2S)-2-(4-bromophenyl)cyclopropane-1-carboxylate | HCID 66578128 | — |
| Produkt | (1R,2R)-2-(4-bromophenyl)Cyclopropanecarboxylic acid | HCID 12586658 | — |
Reaktionsschritte
Another alternative is an enantioselective cyclopropanation using for example a bis-oxazoline chiral ligand/copper complex and diazoacetate (Evans et al. J. Am. Chem. Soc. 1991, 113, 726) to prepare optically active ethyl 2-(cis)-(4-bromophenyl)cyclopropanecarboxylate from 4-bromostyrene. Selective hydrolysis of the mixture of cis and trans isomer with LiOH (1 eq based on trans isomer) gave 2-(trans)-(4-bromophenyl)cyclopropanecarboxylic acid (used in EXAMPLE 1) and the desired ethyl 2-(cis)-(4-bromophenyl)cyclopropanecarboxylate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07342024B2 |
| Quelldatensatz | uspto-grants-2008_03 |
| ORD ID | ord-c8072d8a60b34902a2cdca1dc5110345 |
| Quellennotiz | uspto-grants-2008_03 |