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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1409549생성일: 2026년 10월 26일

4-Aminotetrahydro-2H-pyran-4-carboxylic acid hydrochloride → Methyl 4-aminooxane-4-carboxylate

https://huagongshe.com/reaction/1409549

반응식

참여 물질

역할이름HCID투입량
반응물4-Aminotetrahydro-2H-pyran-4-carboxylic acid hydrochlorideHCID 2734400—
반응물trimethylsilyldiazomethane Et2OHCID 23159941—
용매MethanolHCID 887—
생성물Methyl 4-aminooxane-4-carboxylateHCID 1869831499%

반응 단계

To a solution of 4-amino-4-carboxy-tetrahydropyrane hydrochloride (2 g) in methanol was added dropwise a solution of 2M trimethylsilyldiazomethane-diethylether (33 mL) under ice-cooling, and the mixture was stirred at room temperature for 4 days. The reaction mixture was concentrated in vacuo, and the resultant crude product was dissolved in hexane-diethylether (1 mL/1 mL), and thereto was added an aqueous 4N hydrochloric acid. The precipitates were collected by filtration to give 4-amino-4-methoxycarbonyl-tetrahydropyrane (2.13 g, yield: 99%) as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921380B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-c6845010739e41f19e1c9c8429a37b52
출처 메모uspto-grants-2014_12