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HRID 128586作成日:2026年10月25日

Diethyl Ether → Methyl 2-methoxy-4-(1-acetyl-4-piperidyloxy)phenylacetate

https://huagongshe.com/reaction/128586

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Potassium HydroxideHCID 14797—
反応物Urea, (nitrosomethyl)-HCID 104823—
反応物2-Methoxy-4-(1-acetyl-4-piperidyloxy)benzoyl chlorideHCID 18914181—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-methoxy-4-(1-acetyl-4-piperidyloxy)phenylacetateHCID 18914188—

反応手順

A mixture of ether (14 ml) and 40% aqueous potassium hydroxide (4.2 ml) was cooled in ice. N-Nitrosomethylurea (1.4g) was added in portions with gentle swirling over 30 min. The ether layer was decanted and dried over solid potassium hydroxide for 15 min. The ether solution was decanted, then cooled in an ice bath. A solution of 2-methoxy-4-(1-acetyl-4-piperidyloxy)benzoyl chloride (0.58 g, 1.86 mmol) in THF (3 ml) was added dropwise and the mixture was stirred at ambient temperature for 2 hours. Nitrogen was passed through the mixture for 1 hour, and the solution was then concentrated in vacuo. The residue was dissolved in methanol and treated with freshly prepared silver oxide (48 mg), and the mixture was heated at reflux for 30 min. Three additional lots of 100 mg of silver oxide were added with 1 hour reflux following each. The mixture was cooled and filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed on silica gel eluted with 2%, followed by 4% methanol in methylene chloride. The product fractions were combined and evaporated to dryness in vacuo to give methyl 2-methoxy-4-(1-acetyl-4-piperidyloxy)phenylacetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464788
出典データセットuspto-grants-1995_11
ORD IDord-d53cc10045f340e38f237867eae66b4a
出典メモuspto-grants-1995_11