참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ninhydrin | HCID 10236 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | (2R)-2-amino-3-(trimethylsilyl)propanoic acid | HCID 11008231 | — |
| 반응물 | Boron, trifluoro(methanol)-, (T-4)- | HCID 11062313 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Dichloromethane methanol | HCID 21226129 | — |
| 생성물 | Methyl (R)-2-Amino-3-(trimethylsilyl)propanoate | HCID 59302397 | 92% |
반응 단계
3-Trimethylsilyl alanine (J. Organomet. Chem., 628, (2001), 183–194; 19 mg, 0.118 mmol) was mixed with 3 ml BF3-MeOH (14%, 3.7 mmol) in a sealed tube and heated to 70° C. Analysis was performed using TLC (MeOH:DCM 1:9, stained w. ninhydrine in ethanol). The mixture was heated for 3 h and was then cooled to ambient temperature. The mixture was poured into a mixture of 3 ml EtOAc and 2 ml water containing Na2CO3. More Na2CO3 (5%-aq) was added until pH ca 7. The aqueous phase was washed with EtOAc (2×3 ml). The combined organic layers were washed with brine (1 ml), dried with Na2SO4 and evaporated. The product was obtained as a white film. Mass: 19 mg (92% yield). NMR (CDCl3): 0.1 (s, 9H), 1.2–1.4 (m, 2H), 3.8 (s, 3H), 4.2 (brs, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07132416B2 |
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| 출처 데이터셋 | uspto-grants-2006_11 |
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| ORD ID | ord-5929ac61b44f44a68d65dad6554dcc85 |
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| 출처 메모 | uspto-grants-2006_11 |
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