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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784150Generated: October 28, 2026

Toluene → HCID 22600462, compound

https://huagongshe.com/reaction/1784150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(2-Methoxy-ethoxymethyl)-6-trifluoromethyl-nicotinic acidHCID 11334953—
ReactantHCID 57591516HCID 57591516—
CatalystZincchlorideHCID 3007855—
SolventDichloromethaneHCID 6344—
ProductHCID 22600462HCID 22600462—

Reaction Steps

A mixture of 200 mg (1.15 mmol) of 4-chlorobicyclo[3.2.1]oct-3-en-2-one, (Preparation Example P2) 16 mg (0.12 mmol) of ZnCl2, 324 mg (1.15 mmol) of 2-methoxyethoxymethyl-6 -trifluoromethylnicotinic acid, 166 mg (1.27 mmol) of diisopropylethylamine and 5 ml of toluene is stirred under a nitrogen atmosphere at room temperature until a clear brown solution having a white sediment is formed. The reaction mixture is then maintained under moderate reflux for 26 hours in an oil bath, with stirring. The reaction mixture is then cooled to ambient temperature and 30 ml of dichloromethane are added. The solution is then washed twice with water (20 ml each time) and then twice with 0.1M hydrochloric acid (20 ml each time) and again twice with water (15 ml each time). After drying the organic solution using magnesium sulfate and concentrating in vacuo, 284 mg of 4-(2-methoxyethoxymethyl-6-trifluoromethyl-pyridin-3-ylcarbonyloxy)-bicyclo[3.2.1]oct-3-en-2-one are obtained in the form of a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501544B2
Source datasetuspto-grants-2009_03
ORD IDord-e08e1cbc6beb424492820e89b8e50368
Source noteuspto-grants-2009_03