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HRID 1861239作成日:2026年10月25日

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

https://huagongshe.com/reaction/1861239

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物Bicyclo(2.2.1)hept-5-ene-2-carbonyl chlorideHCID 98233—
反応物2-Ethyl-2-norbornyl acetateHCID 564393—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物2-Ethyl-2-bicyclo[2.2.1]heptyl 3-hydroxybutanoateHCID 18757336—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物2-(2-Ethyl-2-bicyclo[2.2.1]-heptyloxycarbonyl)propyl 2-norbornene-5-carboxylateHCID 1875733584.9%

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06531627B2
出典データセットuspto-grants-2003_03
ORD IDord-a2f04315e95b434c8d641f0761d1f2b9
出典メモuspto-grants-2003_03