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O-benzyl-L-serine → Propanoic acid, 2-bromo-3-(phenylmethoxy)-, (S)-

HRID 464566
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HRID 464566 반응식
[C:1]1([CH2:7][O:8][CH2:9][C@@H:10]([C:12]([OH:14])=[O:13])N)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br-:15].[Na+].N([O-])=O.[Na+]>S(=O)(=O)(O)O>[Br:15][C@@H:10]([CH2:9][O:8][CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[C:12]([OH:14])=[O:13]
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참가 물질

5

반응물 3

HCID 78457O-benzyl-L-serineHCID 253881Sodium BromideHCID 23668193Sodium Nitrite

생성물 1

HCID 12961659Propanoic acid, 2-bromo-3-(phenylmethoxy)-, (S)-수율 37.9%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

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온도
0 °C

실험 절차

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).

후처리

  1. customThe cooling bath was removed
  2. additionether (250 ml) was added
  3. stirringstirring
  4. waitwas continued overnight at room temperature
  5. extractionThe aqueous layer was extracted repetitively with ether (3×100 ml)
  6. dry with materialthe combined extracts were dried over anhydrous magnesium sulfate
  7. customevaporated under reduced pressure
  8. customto give 25 g of a crude product
  9. customThe product was purified by column chromatography (83:17; petroleum ether:ethyl acetate)

출처 및 근거

ORD 기록
ord-378505d06e3c4158a224f14682c12fae
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04548751

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