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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434197Generated: October 26, 2026

Acetaldehyde → 2-(2-Ethyl-2-bicyclo[2.2.1]-heptyloxycarbonyl)propyl 2-norbornene-5-carboxylate

https://huagongshe.com/reaction/434197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantBicyclo(2.2.1)hept-5-ene-2-carbonyl chlorideHCID 98233—
Reactant2-Ethyl-2-norbornyl acetateHCID 564393—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-Ethyl-2-bicyclo[2.2.1]heptyl 3-hydroxybutanoateHCID 18757336—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product2-(2-Ethyl-2-bicyclo[2.2.1]-heptyloxycarbonyl)propyl 2-norbornene-5-carboxylateHCID 1875733584.9%

Reaction Steps

In 350 ml of methylene chloride was dissolved 74.4 g of 2-ethyl-2-bicyclo[2.2.1]heptyl 3-hydroxybutanoate (which was synthesized by reacting 2-ethyl-2-bicyclo[2.2.1]heptyl acetate with acetoaldehyde in the presence of lithium hexamethyldisilazide). Then 39.0 g of pyridine and a catalytic amount of 4-(N,N-dimethylamino)pyridine were added to the solution, which was stirred under ice cooling. To this reaction mixture below 10° C., 66.8 g of 2-norbornene-5-carboxylic chloride was added dropwise over one hour. After agitation was continued for 3 hours, the reaction solution was worked up in a conventional manner. The resulting oily substance was purified by silica gel column chromatography, obtaining 96.7 g of 2-(2-ethyl-2-bicyclo[2.2.1]-heptyloxycarbonyl)propyl 2-norbornene-5-carboxylate, designated Monomer 1. The yield was 84.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670498B2
Source datasetuspto-grants-2003_12
ORD IDord-95023b1574284f0d8f51d8af64c97ca6
Source noteuspto-grants-2003_12