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HRID 858201作成日:2026年10月25日

Diethyl Ether → 4-(cis-3-Allylcyclohexyloxymethyl)-2-(3-methylphenyl)-5-methyloxazole

https://huagongshe.com/reaction/858201

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Sodium hydrideHCID 24758—
反応物4-Iodomethyl-5-methyl-2-m-tolyloxazoleHCID 21980308—
反応物cis-3-AllylcyclohexanolHCID 58763359—
溶媒DimethylformamideHCID 6228—
生成物4-(cis-3-Allylcyclohexyloxymethyl)-2-(3-methylphenyl)-5-methyloxazoleHCID 68857183—

反応手順

2 g of cis-3-allylcyclohexanol are dissolved in 30 ml of dimethylformamide, and 750 mg of sodium hydride (60% strength suspension in paraffin oil) are added. After 30 minutes, 6.7 g of 4-iodomethyl-5-methyl-2-(3-methylphenyl)oxazole, dissolved in 20 ml of dimethylformamide, are added dropwise. The mixture is stirred at room temperature for 1 hour. 200 ml of methy tert-buthyl ether are then added to the reaction mixture, and the mixture is washed three times with water. The organic phase is dried over magnesium sulfate and the solvent is then removed under reduced pressure. The residue is purified by RP-HPLC. This gives 1.56 g of 4-(cis-3-allylcyclohexyloxymethyl)-2-(3-methylphenyl)-5-methyloxazole as an oil. C21H27NO2 (325.45), MS (ESI): 326 (M+H+), Rf(n-heptane:ethylacetate=2:1)=0.28.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07148246B2
出典データセットuspto-grants-2006_12
ORD IDord-1ea7bf2aa6d04216be5e39b3b71bf910
出典メモuspto-grants-2006_12