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HRID 1168288作成日:2026年10月27日

Oxalyl chloride → HCID 86585303、化合物

https://huagongshe.com/reaction/1168288

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物DiisopropylethylamineHCID 81531—
反応物N-HydroxypropionimidamideHCID 4092053—
反応物ST092333HCID 10932896—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 86585303HCID 8658530388.2%

反応手順

Oxalyl chloride (4 ml, 46 mmol) was added to a solution of (3aS,4S,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxylic acid (Justus Liebigs Ann. Chem., 1974, 11, 1856) (5 g, 23 mmol) in dichloromethane (100 ml). The solution was stirred at room temperature for two hours and then the solvent was evaporated under reduced pressure to yield a white solid. This was dissolved in ethyl acetate (80 ml) and N′-hydroxypropanimidamide (2.63 g, 30 mmol) was added followed by N-ethyldiisopropylamine (8.12 ml, 46 mmol). The reaction mixture was stirred at room temperature for 48 hours and then washed with saturated sodium hydrogencarbonate solution (50 ml) and brine (50 ml). The organic layer was separated, dried (anhydrous magnesium sulphate) and evaporated under reduced pressure to give the product as a dark yellow oil (5.85 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06624158B2
出典データセットuspto-grants-2003_09
ORD IDord-e098c59da3e64362a248b7f904bf4b62
出典メモuspto-grants-2003_09