참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | O-benzyl-L-serine | HCID 78457 | — |
| 반응물 | Sodium Bromide | HCID 253881 | — |
| 반응물 | Sodium Nitrite | HCID 23668193 | — |
| 용매 | Sulfuric Acid | HCID 1118 | — |
| 생성물 | Propanoic acid, 2-bromo-3-(phenylmethoxy)-, (S)- | HCID 12961659 | 37.9% |
반응 단계
A solution of O-(phenylmethyl)-L-serine (21.6 g, 0.108 mol) in aqueous sulfuric acid (786 ml, 2.5N) containing sodium bromide (69.3 g, 6.0 eq) was cooled to 0° C. in an ice bath. Sodium nitrite (21 g, 2.7 eq) was added over 10 minutes, and the solution stirred at 0° C. for one hour. The cooling bath was removed, ether (250 ml) was added, and stirring was continued overnight at room temperature. The aqueous layer was extracted repetitively with ether (3×100 ml), and the combined extracts were dried over anhydrous magnesium sulfate and evaporated under reduced pressure to give 25 g of a crude product. The product was purified by column chromatography (83:17; petroleum ether:ethyl acetate) to yield the title compound (10.6 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04548751 |
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| 출처 데이터셋 | uspto-grants-1985_10 |
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| ORD ID | ord-378505d06e3c4158a224f14682c12fae |
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| 출처 메모 | uspto-grants-1985_10 |
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