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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271293생성일: 2026년 10월 26일

4-Aminotetrahydro-2H-pyran-4-carboxylic acid hydrochloride → (4-Aminooxan-4-yl)methanol

https://huagongshe.com/reaction/271293

반응식

참여 물질

역할이름HCID투입량
반응물4-Aminotetrahydro-2H-pyran-4-carboxylic acid hydrochlorideHCID 2734400—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물(4-Aminooxan-4-yl)methanolHCID 18316484—

반응 단계

(4-Amino-tetrahydropyran-4-yl)-methanol is prepared by adding LAH (99%, 1.2 g), portionwise, to a stirred mixture of 4-aminotetrahydropyran-4-carboxylic acid hydrochloride (2.0 g, 11.0 mmol) in THF (30 mL) at 0° C. Upon completion of addition, the reaction mixture is warmed to room temperature and stirred for 1 hour. The reaction mixture is cooled to 0° C. and cautiously quenched by the portionwise addition of Na2SO4.10H2O (4 g). The reaction mixture is diluted with ethyl acetate, warmed to room temperature, and filtered through Celite to give the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452895B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-955178be882b404683e51d66c5fa93f9
출처 메모uspto-grants-2008_11