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HRID 1280648생성일: 2026년 10월 26일

Borohydride → (R)-2-Amino-3-cyclohexylpropan-1-ol

https://huagongshe.com/reaction/1280648

반응식

참여 물질

역할이름HCID투입량
반응물BorohydrideHCID 28123—
반응물Sodium borohydrideHCID 4311764—
반응물ethyl (2R)-2-amino-3-cyclohexylpropanoateHCID 86584436—
용매EthanolHCID 702—
생성물(R)-2-Amino-3-cyclohexylpropan-1-olHCID 40432407105.5%

반응 단계

The process is performed as in Example 1, starting with 6.2 g of ethyl (2R)-2-amino-3-cyclohexylpropionate and 1.93 g of sodium borohydride in 120 cm2 of absolute ethanol at about 5° C. for 10 minutes. The medium is warmed to room temperature and stirred for a further 3 h 30 minutes. After cooling again to about 5° C. and addition of a further 40.94 g of borohydride, followed by stirring at a temperature in the region of 20° C. for 65 hours, the reaction medium is concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. A solid is obtained, which is purified by chromatography under a pressure of argon (100 kPa) on a column of silica gel (particle size 40-63μ; 320 g), eluting with pure methanol. The fractions containing the expected product are collected. These fractions are combined and then concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. 5.16 g of (2R)-2-amino-3-cyclohexyl-1-propanol are obtained in the form of a sticky white solid. (Rf=0.25 in methanol on a Merck 60F254R silica plate)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06451821B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-c706560a801e4b7da16c8f955f18232a
출처 메모uspto-grants-2002_09