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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → 769169-13-3

HRID 1594279
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HRID 1594279 반응식
[N:1]([C@@H:4]([C@H:8]([CH3:14])[CH2:9][C:10]([F:13])([F:12])[F:11])[C:5]([OH:7])=[O:6])=[N+]=[N-].C(O)(=O)C>[Pd].O>[F:11][C:10]([F:12])([F:13])[CH2:9][C@@H:8]([CH3:14])[C@@H:4]([C:5]([OH:7])=[O:6])[NH2:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 86594488HCID 86594488, 화합물

생성물 1

HCID 86594487769169-13-3수율 96%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 962Water용매

실험 절차

(2S,3R)-2-azido-5,5,5-trifluoro-3-methylpentanoic acid (3.2 g, 17.27 mmol), 10% palladium on carbon (0.79 g), glacial acetic acid (37 mL) and water (90 mL) was placed under an atmosphere of hydrogen (40 psi) and shaken on Parr hydrogenator. After 20 h, the reaction mixture was filtered through a pad of the Celite® reagent which was rinsed well with H2O (20 mL). The filtrate was concentrated under reduced pressure to produce a white solid. The solid was triturated with EtOAc (200 mL), filtered and washed once more with EtOAc (200 mL) then air dried to give 5,5,5-trifluoro-L-alloisoleucine as a white solid (2.7 g, 96%). Mass Spectrum (−ESI): 184 (M−H)−.

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후처리

  1. filtrationthe reaction mixture was filtered through a pad of the Celite® reagent which
  2. washwas rinsed well with H2O (20 mL)
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. customto produce a white solid
  5. customThe solid was triturated with EtOAc (200 mL)
  6. filtrationfiltered
  7. washwashed once more with EtOAc (200 mL)
  8. customair dried

출처 및 근거

ORD 기록
ord-cba777340a174a7c8e391cae7f458ade
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07300951B2

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