HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenylethanol → HCID 131714337, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenylethanol | HCID 6054 | — |
| Reactant | (2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrile | HCID 9837437 | — |
| Reactant | (S)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[Z-2-carboxy-ethenyl]-cyclopropanecarboxylate | HCID 13093798 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 131714337 | HCID 131714337 | — |
Reaction Steps
Using the procedure of Step F of Example 9the ester of Step A of Example 31 after reaction with phenethanol and (S)α-cyano-3-phenoxy-benzyl alcohol was reacted to obtain (S) -cyano-3-phenoxy-benzyl (IR,cis) 2,2-dimethyl-3[(Z) 3-oxo -3-phenethoxy-1-propenyl]-cyclopropane-carboxylate with a specific rotation of [α]D20 =+46°±2.5° (c=0.5% in benzene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04883806 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-95da9d843c724a998bb9bd980b0dbebc |
| Source note | uspto-grants-1989_11 |