참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromide ion | HCID 259 | — |
| 반응물 | L-Valine | HCID 6287 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (S)-2-(4-bromobenzyl)amino-3-methylbutyric acid | HCID 11673643 | 153.4% |
반응 단계
52 mL (0.21 mol) of N,O-bistrimethylsilylacetamide is added under nitrogen atmosphere to a mixture made up of 23.5 g (0.20 mol) of L-valine and 38.5 mL (0.22 mol) of diisopropylethylamine in 12.5 mL of DMF. After 1 h at 80° C. the suspension changes to a clear solution. Then, in portions and controlling exothermy, 50 g (0.20 mol) of 4-bromobenzylo bromide is added and left to react at 80° C. for 2 h. The mixture is cooled to 20-25° C., 250 mL of toluene and a solution made up of 250 mL of water and 80 mL of NaOH 40% are added. The resulting aqueous phase is washed twice with 100 mL of AcOEt, the remains of solvent distilled and taken to pH 6-7 with HCl 3N. The solid obtained is filtered with 250 mL of IPA to give 43.9 g (76.5%) of N-(4-bromobenzyl)-L-valine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728021B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-145a239c04c24a43b4d3485f843fcd6d |
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| 출처 메모 | uspto-grants-2010_06 |
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