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Water → (2E,4S)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-2-hexenoic acid

HRID 714565
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HRID 714565 반응식
[Li+].[OH-].[CH3:3][C:4]([O:7][C:8]([NH:10][C@@H:11]([CH2:18][CH3:19])/[CH:12]=[CH:13]/[C:14]([O:16]C)=[O:15])=[O:9])([CH3:6])[CH3:5].O>C1COCC1.CO>[CH3:6][C:4]([O:7][C:8]([NH:10][C@@H:11]([CH2:18][CH3:19])/[CH:12]=[CH:13]/[C:14]([OH:16])=[O:15])=[O:9])([CH3:3])[CH3:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 962WaterHCID 3939Lithium HydroxideHCID 86666383HCID 86666383, 화합물

생성물 1

HCID 86704312(2E,4S)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-2-hexenoic acid수율 107.7%

시약·촉매·용매 2

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

LiOH (2.95 g, 123 mmol) was added to a solution of methyl (2E,4S)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-2-hexenoate (6 g, 24.66 mmol) in THF (50 mL), MeOH (10.00 mL), and water (50.0 mL). The reaction was stirred overnight at RT. After 18.5 h, the reaction mixture was concentrated under reduced pressure to remove the THF and MeOH. Water (40 mL) was added, and aqueous mixture was adjusted to pH=3 with 6 M aq. HCl, as measured by pH paper. EtOAc (80 mL) was added, the layers were separated, and the aqueous layer was extracted with EtOAc (2×40 mL). The combined organic layers were dried over Na2SO4, concentrated under reduced pressure, and dried under high vacuum, giving 6.09 g of the title compound. LC-MS m/z 230 (M+H)+, 0.77 min (ret time).

후처리

  1. waitAfter 18.5 h
  2. concentrationthe reaction mixture was concentrated under reduced pressure
  3. customto remove the THF and MeOH
  4. additionWater (40 mL) was added
  5. additionEtOAc (80 mL) was added
  6. customthe layers were separated
  7. extractionthe aqueous layer was extracted with EtOAc (2×40 mL)
  8. dry with materialThe combined organic layers were dried over Na2SO4
  9. concentrationconcentrated under reduced pressure
  10. customdried under high vacuum

출처 및 근거

ORD 기록
ord-fdc1cd8198524bada9faa051c39a4d9b
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187461B2

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