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Hydrochloric Acid → (3S,5S)-3-amino-3,5-dimethyl-heptanoic acid

HRID 349807
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 349807
C[O:2][C:3](=[O:19])[CH2:4][C@@:5]([CH3:18])([NH:11][S@](C(C)(C)C)=O)[CH2:6][C@@H:7]([CH3:10])[CH2:8][CH3:9].Cl>CC(C)=O.O>[NH2:11][C@@:5]([CH3:18])([CH2:6][C@@H:7]([CH3:10])[CH2:8][CH3:9])[CH2:4][C:3]([OH:19])=[O:2]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 313Hydrochloric AcidHCID 86597957(3S,5S)-3,5-Dimethyl-3-((S)-2-methyl-propane-2-sulfinylamino)-heptanoic Acid Methyl Ester

Produkt 1

HCID 86597958(3S,5S)-3-amino-3,5-dimethyl-heptanoic acidAusbeute 77 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 180AcetoneLösungsmittelHCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

A mixture of (3S,5S)-3,5-dimethyl-3-((S)-2-methyl-propane-2-sulfinylamino)-heptanoic acid methyl ester (0.4 g, 1.37 mmol) and concentrated hydrochloric acid (7.6 mL) in acetone (10 mL) was refluxed for 3 hours. The solvents were stripped under reduced pressure. The residue was dissolved in water (10 mL) and extracted by EtOAc (2×15 mL). The aqueous phase was evaporated to dryness. The residue was dissolved in a mixture of water (10 mL) and triethylamine (0.5 mL). The mixture was stirred at 40° C. for 20 minutes and then was evaporated to dryness. The residue was washed thoroughly with acetonitrile, filtered, and dried under vacuum to give the final product, (3S,5S)-3-amino-3,5-dimethyl-heptanoic acid (0.182 g, 77% yield) as a white solid. m.p. 215–217° C.: 1H NMR (CDCl3) δ 4.85 (s, 3H), 2.38 (m, 2H), 1.75 (m, 1H), 1.39 (m, 4H), 1.35(s, 3H), 0.98 (d, J=6.6 Hz, 3H), 0.90 (t, J=7.5 Hz, 3H); MS (APCl) (M+1)+ 174.1.

Aufarbeitung

  1. temperaturewas refluxed for 3 hours
  2. extractionextracted by EtOAc (2×15 mL)
  3. customThe aqueous phase was evaporated to dryness
  4. dissolutionThe residue was dissolved in a mixture of water (10 mL) and triethylamine (0.5 mL)
  5. customwas evaporated to dryness
  6. washThe residue was washed thoroughly with acetonitrile
  7. filtrationfiltered
  8. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-3e83cc1a80e444acb5be55aad1da3fbe
Quelldatensatz
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07179934B2

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