戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1452073作成日:2026年10月25日

Carbon Dioxide → Propiolic Acid

https://huagongshe.com/reaction/1452073

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物Chloromethyl Methyl EtherHCID 7864—
反応物5-(Bromomethyl)-3-methoxy-1,2-oxazoleHCID 10845405—
反応物3-Diphenylmethoxy-4-iodomethyl-1,2,5-thiadiazoleHCID 22906284—
反応物HCID 178462446HCID 178462446—
溶媒TetrahydrofuranHCID 8028—
生成物Propiolic AcidHCID 10110—
生成物HCID 178462446HCID 178462446—

反応手順

Dibromoolefin intermediate XIX is then converted to ethynyl intermediate XX. Treatment of the dibromoolefin intermediate with about two equivalents of n-butyllithium produces the lithium acetylide XX, wherein R13 is Li. This transformation is typically carried out in a polar organic solvent, such as tetrahydrofuran, at a temperature of about -78° C. to about 25° C. The lithium acetylide is reacted with electrophiles, such as methoxymethyl chloride, 5-bromomethyl-3-methoxyisoxazole, 3-diphenylmethoxy-4-iodomethyl-1,2,5-thiadiazole, carbon dioxide, tetrazole disulfide, and the like, to prepare the formula I compounds. In a typical example, the lithium acetylide is treated with solid CO2 at a temperature of about -78° C. to about -60° C. to produce propargylic acid intermediate XX wherein R13 is CO2H. This compound may be further modified as described herein.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05606062
出典データセットuspto-grants-1997_02
ORD IDord-574031d5700748da82256e72eb159a91
出典メモuspto-grants-1997_02