돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128590생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/128590

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Potassium HydroxideHCID 14797—
반응물Urea, (nitrosomethyl)-HCID 104823—
반응물2-methoxy-4-(1-Boc-4-piperidyloxy)benzoyl chlorideHCID 18914155—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-methoxy-4-(1-Boc-4-piperidyloxy)phenylacetateHCID 18914175—

반응 단계

A mixture of ether (66 ml) and 40% aqueous potassium hydroxide (20 ml) was cooled in ice. N-Nitrosomethylurea (6.6 g) 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, and the decanted solution was cooled in an ice bath. A solution of 2-methoxy-4-(1-Boc-4-piperidyloxy)benzoyl chloride (3.26 g, 8.8 mmol) in THF (6 ml) was added dropwise and the mixture was stirred in the cold for 15 min and at ambient temperature for 3.5 hours. Nitrogen was passed through the mixture for 1 hour, and the solution was then concentrated in vacuo. A portion (930 mg) of the residue was dissolved in methanol and heated to reflux, and a solution of silver benzoate (200 mg) in triethylamine (2 ml) was added in five 0.1 ml portions at intervals of eight minutes. A sixth portion was added after an additional forty minutes' reflux, and after another five minutes, a seventh portion. After a final 30 minutes' reflux, the mixture was cooled and filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed on silica gel eluted with 3%, followed by 5% methanol in methylene chloride. The product fractions were combined and evaporated to dryness in vacuo to give methyl 2-methoxy-4-(1-Boc-4-piperidyloxy)-phenylacetate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464788
출처 데이터셋uspto-grants-1995_11
ORD IDord-1759206d62554e9db68d9407fb9fe857
출처 메모uspto-grants-1995_11