戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1279844作成日:2026年10月26日

1,1'-Carbonyldiimidazole → tert-butyl (3R)-6-cyclohexyl-3-(3-methyl-1,2,4-oxadiazol-5-yl)hexanoate

https://huagongshe.com/reaction/1279844

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物(2R)-2-[2-(tert-butoxy)-2-oxoethyl]-5-cyclohexylpentanoic acidHCID 9835906—
反応物HCID 178465666HCID 178465666—
溶媒DichloromethaneHCID 6344—
生成物tert-butyl (3R)-6-cyclohexyl-3-(3-methyl-1,2,4-oxadiazol-5-yl)hexanoateHCID 5990976457.2%

反応手順

A solution of (2R)-2-[2-(tert-butoxy)-2-oxoethyl]-5-cyclohexylpentanoic acid (Preparation 1) (596 mg, 2.00 mmol) in dichloromethane (8ml) was treated with 1,1′-carbonyldiimidazole (364 mg, 2.25 mol) and the solution was stirred at room temperature for 15 minutes. The N-hydroxyacetamidine (Chem.Ber.; 17; 1884; 2746) (148 mg, 2.00 mmol) was then added and the mixture was stirred for 1 hour. The solvent was removed under reduced pressure and the residue was heated neat under a nitrogen atmosphere for 90 minutes. The crude product was then purified by column chromatography on silica gel eluting with dichloromethane to afford the title compound (385 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06448278B2
出典データセットuspto-grants-2002_09
ORD IDord-0fd2fe6cb17647cd977ad92b3b7c3250
出典メモuspto-grants-2002_09