참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetyl chloride | HCID 6367 | — |
| 반응물 | 2-Amino-4-bromobutanoic acid hydrobromide | HCID 13877992 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Methyl 4-bromo-2-amino-butyrate hydrochloride | HCID 13877993 | 82% |
반응 단계
Acetyl chloride (61 mL, 860 mmol) was added dropwise to 200 mL of MeOH at 0° C. The mixture was stirred at room temperature for 30 min, and 22.5 g (124 mmol) of 2-amino-4-bromo-butyric acid hydrobromide was added. The mixture was stirred overnight and concentrated. The residue was washed with Et2O to provide 23.5 g (82%) of methyl 4-bromo-2-amino-butyrate hydrochloride. A solution of 27.7 g (330 mmol) of NaHCO3 in 100 mL of water was slowly added to 19.2 g (82.5 mmol) of this material along with 21.6 g (99.0 mmol) of Boc2O in 140 mL of 1,4-dioxane at 0° C., The mixture was warmed to room temperature and stirred overnight. N,N-dimethylpropane-1,3-diamine (5 mL) was added to the mixture, and stirring was continued for 20 min. The mixture was diluted with water then extracted twice with EtOAc. The extracts were washed with water, 1M NaHSO4, and brine, and then combined, dried with Na2SO4, filtered, and concentrated to provide 21.5 g (88%) of 4-bromo-2-tert-butoxycarbonylamino-butyric acid methyl ester as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08552205B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-e0a3485e761b4f3bac876a1dfdae074c |
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| 출처 메모 | uspto-grants-2013_10 |
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