HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaR)- → HCID 13105999, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaR)- | HCID 156232 | — |
| Edukt | HCID 54557330 | HCID 54557330 | — |
| Edukt | [Z-2-(methoxycarbonyl)-ethenyl]-cyclopropane carboxylic acid | HCID 131713081 | — |
| Produkt | HCID 13105999 | HCID 13105999 | — |
Reaktionsschritte
Using the procedure of Step D of Example 1, 1.5 g of (1R, cis) 2,2-dimethyl-3-([Z-2-(methoxycarbonyl)-ethenyl]-cyclopropane carboxylic acid and 1.9 g of (R)α-cyano-3-phenoxybenzyl alcohol were reacted to obtain 4.3 g of raw product. The latter was chromatographed over silica gel and was eluted with a 9-1 cyclohexane-ethyl acetate mixture to obtain 2.5 g of (R)α-cyano-3-phenoxy-benzyl (1R,cis) 2,2-dimethyl-3-[Z-2-(methoxycarbonyl)-ethenyl]-cyclopropane carboxylate with a specific rotation of [α]D20 =+23.5°±2.5° (c=0.5% in benzene).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04402972 |
| Quelldatensatz | uspto-grants-1983_09 |
| ORD ID | ord-f639dc4048f44a5d88fc41ce91814ba8 |
| Quellennotiz | uspto-grants-1983_09 |