Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277528Generated: November 1, 2026

3-Phenoxybenzaldehyde → Sodium

https://huagongshe.com/reaction/1277528

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PhenoxybenzaldehydeHCID 38284—
ReactantSodiumHCID 5360545—
ReactantHCID 131712291HCID 131712291—
CatalystZincchlorideHCID 3007855—
ProductSodiumHCID 5360545—
ProductHCID 86737846HCID 86737846—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04277617
Source datasetuspto-grants-1981_07
ORD IDord-e709cd144fa142a783461d423f6e1dd1
Source noteuspto-grants-1981_07