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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128586생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/128586

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Potassium HydroxideHCID 14797—
반응물Urea, (nitrosomethyl)-HCID 104823—
반응물2-Methoxy-4-(1-acetyl-4-piperidyloxy)benzoyl chlorideHCID 18914181—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-methoxy-4-(1-acetyl-4-piperidyloxy)phenylacetateHCID 18914188—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464788
출처 데이터셋uspto-grants-1995_11
ORD IDord-d53cc10045f340e38f237867eae66b4a
출처 메모uspto-grants-1995_11