참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Borohydride | HCID 28123 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | ethyl (2R)-2-amino-3-cyclohexylpropanoate | HCID 86584436 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | (R)-2-Amino-3-cyclohexylpropan-1-ol | HCID 40432407 | 105.5% |
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 cm3 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06699895B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-15ed5e09c0304ee0806312e42daad942 |
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| 출처 메모 | uspto-grants-2004_03 |
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