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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784152Generated: October 30, 2026

Diisopropylethylamine → HCID 22600462, compound

https://huagongshe.com/reaction/1784152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(2-Methoxy-ethoxymethyl)-6-trifluoromethyl-nicotinic acidHCID 11334953—
ReactantHCID 57591513HCID 57591513—
CatalystZincchlorideHCID 3007855—
SolventChlorobenzeneHCID 7964—
ProductHCID 22600462HCID 22600462—

Reaction Steps

A mixture of 27 g of a 6.2% solution of 4-bromobicyclo[3.2.1]oct-3-en-2-one (Preparation Example P1) in chlorobenzene, 110 mg of ZnCl2, 2.34 g of 2-methoxyethoxymethyl-6-trifluoromethylnicotinic acid and 1.2 g of Hünig's base is stirred at room temperature under a nitrogen atmosphere until a dark-brown solution is formed. The reaction mixture is then maintained under moderate reflux for 19 hours in an oil bath, with stirring. The mixture is then divided into 2 portions. To one portion there are added a further 1.12 g of 2-methoxyethoxymethyl-6-trifluoromethylnicotinic acid, 0.06 g of ZnCl2 and 0.6 g of Hünig's base. The reaction mixture is then maintained under moderate reflux for 12 hours in an oil bath, with stirring. The solution is then washed twice with 0.1M hydrochloric acid (20 ml each time) and twice with water (20 ml each time). After drying the organic solution using magnesium sulfate and concentrating in vacuo, 3.9 g 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-490092c910054855818fdd351ad58b33
Source noteuspto-grants-2009_03