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Hydrochloric Acid → t-butoxycarbonylmethyl 5-(Boc-amino)-4-oxopentanoate

HRID 1771022
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HRID 1771022 반응식
C(N(CC)CC)C.[C:8]([NH:15][CH2:16][C:17](=[O:23])[CH2:18][CH2:19][C:20]([OH:22])=[O:21])([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9].Br[CH2:25][C:26]([O:28][C:29]([CH3:32])([CH3:31])[CH3:30])=[O:27].Cl>C(OCC)(=O)C>[C:8]([NH:15][CH2:16][C:17](=[O:23])[CH2:18][CH2:19][C:20]([O:22][CH2:25][C:26]([O:28][C:29]([CH3:32])([CH3:31])[CH3:30])=[O:27])=[O:21])([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 79177tert-Butyl bromoacetateHCID 179898205-((tert-Butoxycarbonyl)amino)-4-oxopentanoic acid

생성물 1

HCID 90034544t-butoxycarbonylmethyl 5-(Boc-amino)-4-oxopentanoate수율 89%

시약·촉매·용매 1

HCID 8857
Ethyl Acetate
용매

실험 절차

Triethylamine (2.22 g; 22.0 mmol) was added dropwise to a stirred solution of 5-(Boc-amino)-4-oxopentanoic acid (4.62 g; 20.0 mmol) and t-butyl bromoacetate (4.30 g; 22.0 mmol) in ethyl acetate (60 mL) under argon at ambient temperature. The mixture (slurry) was refluxed for 17 h, then cooled to ambient temperature, poured into 0.5 M HCl (100 mL) and shaken thoroughly. The aqueous portion was extracted with ethyl acetate (2×20 mL). The combined organic solutions were washed with saturated NaHCO3 solution (1×20 mL) and saturated NaCl solution (1×20 mL) then dried (MgSO4), filtered and evaporated. Evaporation resulted in an amber oil that was purified by flash chromatography on a 40×55-mm silica gel 60 column eluted with ethyl acetate-hexane (1:1) (600 mL), collecting 5×100 mL fractions. Evaporation of fractions 1 and 2 resulted in 6.15 g (89%) product (yellow oil).

후처리

  1. temperatureThe mixture (slurry) was refluxed for 17 h
  2. extractionThe aqueous portion was extracted with ethyl acetate (2×20 mL)
  3. washThe combined organic solutions were washed with saturated NaHCO3 solution (1×20 mL) and saturated NaCl solution (1×20 mL)
  4. dry with materialthen dried (MgSO4)
  5. filtrationfiltered
  6. customevaporated
  7. customEvaporation
  8. customresulted in an amber oil that
  9. customwas purified by flash chromatography on a 40×55-mm silica gel 60 column
  10. washeluted with ethyl acetate-hexane (1:1) (600 mL)
  11. customcollecting 5×100 mL fractions
  12. customEvaporation of fractions 1 and 2

출처 및 근거

ORD 기록
ord-043ee78e928c4da7b67a8a64d9a49c80
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09249086B2

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