Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 131712291 | HCID 131712291 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | Sodium | HCID 5360545 | — |
| Product | HCID 86737846 | HCID 86737846 | — |
Reaction Steps
A mixture of 8 g of 3-phenoxy-benzaldehyde and 15.5 g of 1R, trans 2,2-dimethyl-3-(1',2'-dibromo-2',2'-dichloroethyl)-cyclopropane-1-carboxylic acid chloride was warmed to obtain a homogeneous liquid and the mixture was cooled to 20° C. 0.150 g of anhydrous zinc chloride were added thereto and the mixture was stirred at 20° C. for 17 hours to obtain raw RS α-chloro-3-phenoxy-benzyl 1R, trans 2,2-dimethyl-3-(1',2'-dibromo-2',2'-dichloroethyl)-cyclopropane-1-carboxylate whose IR spectrum showed an absorption at 1750 cm-1 (carbonyl) andwhose RMN Spectrum showed the absence of an aldehydic proton.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04277617 |
|---|
| Source dataset | uspto-grants-1981_07 |
|---|
| ORD ID | ord-e709cd144fa142a783461d423f6e1dd1 |
|---|
| Source note | uspto-grants-1981_07 |
|---|