戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1377654作成日:2026年10月25日

Hydrochloric Acid → (Z)-2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]-2-propenyl]-1,3-dioxane

https://huagongshe.com/reaction/1377654

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium hydrideHCID 24758—
反応物2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromideHCID 2724168—
反応物4-[2-(5-Methyl-2-phenyloxazol-4-yl)ethoxy]benzaldehydeHCID 10757106—
溶媒DimethylformamideHCID 6228—
生成物(Z)-2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]-2-propenyl]-1,3-dioxaneHCID 1181157177.3%

反応手順

Sodium hydride (60% in oil, 0.78 g) was added in limited amounts, at room temperature, to a solution of [2-(1,3-dioxan-2-yl)ethyl]triphenylphosphonium bromide (8.9 g) in N,N-dimethylformamide (100 ml). The mixture was stirred for 30 minutes at the same temperature range, to which was added 4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzaldehyde (5.0 g). The mixture was stirred for 15 minutes at room temperature, then for 5 hours at 70° C. The reaction mixture was poured into ice-water, which was acidified with 2N HCl, followed by extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4). The residue was purified by means of a silica gel column chromatography. From the fractions eluted with hexane - ethyl acetate (3:1), (Z)-2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]-2-propenyl]-1,3-dioxane (5.1 g, 77%) was obtained as an oily product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05665748
出典データセットuspto-grants-1997_09
ORD IDord-af347065ca4e40ea95b28c1b9aa53870
出典メモuspto-grants-1997_09