(1S,2R)-(-)-1-Amino-2-indanol → (3S)-3-(4-Hydroxyphenyl)-4-hexynoic acid

HRID 1993018

Reaktionsgleichung

Reaktionsgleichung von HRID 1993018
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:13]#[C:14][CH3:15])[CH2:9][C:10]([OH:12])=[O:11])=[CH:4][CH:3]=1.N[C@H]1C2C(=CC=CC=2)C[C@H]1O>CC(O)C>[OH:1][C:2]1[CH:3]=[CH:4][C:5]([C@@H:8]([C:13]#[C:14][CH3:15])[CH2:9][C:10]([OH:12])=[O:11])=[CH:6][CH:7]=1

Komponenten

4

Edukt 2

HCID 9866743(1S,2R)-(-)-1-Amino-2-indanolHCID 598551363-(4-Hydroxyphenyl)hex-4-ynoic acid

Produkt 1

HCID 59855121(3S)-3-(4-Hydroxyphenyl)-4-hexynoic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3776IsopropanolLösungsmittel2×

Versuchsvorschrift

A 5 L RB flask was charged with compound 1.3 (66.4 g, 325 mmol) and 2-propanol (1 L) and then heated to 70° C. (1S,2R)-1-amino-2-indanol (46.1 g, 309 mmol) was dissolved in 2-propanol (1 L) with gentle warming. The solution of amine was added to the dissolved carboxlic acid and the resulting solution was allowed to cool to room temperature. After 16 h, the crystals were collected and dried. The salt was re-suspended in 2 L of 2-propanol and dissolved by heating to reflux. After allowing to cool to room temperature, the salt was collected after 16 h. A small sample of the salt was decomposed with aqueous acid and the free carboxylic acid was analyzed by chiral HPLC (Daicel ChiralPAK AD-H column, eluant: 0.1% TFA in 90:10 hexanes:2-propanol) and was found to have 75% ee. The salt was re-suspended in 1.5 L of 2-propanol and dissolved by heating to reflux. After allowing to cool to room temperature, the salt was collected after 16 h. This material was found to have 96% ee by chiral HPLC. This material was suspended in ethyl acetate (300 mL) and water (100 mL). Saturated aqueous KHSO4 (100 mL) was added with vigorous mixing. After two clear layers were obtained, the layers were separated and the aqueous layer extracted with ethyl acetate (100 mL). The combined extracts were washed with saturated brine, dried over MgSO4, filtered, and concentrated to a light yellow oil which crystallized on drying in vacuo. Compound 1.4 was obtained as an off-white solid (23.5 g, 35%).

Aufarbeitung

  1. customthe crystals were collected
  2. customdried
  3. dissolutiondissolved
  4. temperatureby heating to reflux
  5. temperatureto cool to room temperature
  6. customthe salt was collected after 16 h
  7. dissolutiondissolved
  8. temperatureby heating to reflux
  9. temperatureto cool to room temperature
  10. customthe salt was collected after 16 h
  11. additionSaturated aqueous KHSO4 (100 mL) was added with vigorous mixing
  12. customAfter two clear layers were obtained
  13. customthe layers were separated
  14. extractionthe aqueous layer extracted with ethyl acetate (100 mL)
  15. washThe combined extracts were washed with saturated brine
  16. dry with materialdried over MgSO4
  17. filtrationfiltered
  18. concentrationconcentrated to a light yellow oil which
  19. customcrystallized
  20. customon drying in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d8d8b230233e492ab5dbd6e513fd0d91
Quelldatensatz
uspto-grants-2010_01
Patentnummer
US07649110B2

Verknüpfte Notizen

Wird geladen…