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Isopropyl Acetate → 1H-Inden-2-amine, 5-bromo-2,3-dihydro-, (2R)-

HRID 1814778
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1814778
C(OC(C)C)(=O)C.[C@]12(CS(O)(=O)=O)C(C)(C)C(CC1)CC2=O.[C@]12(CS(O)(=O)=O)C(C)(C)C(CC1)CC2=O.[Br:38][C:39]1[CH:40]=[C:41]2[C:45](=[CH:46][CH:47]=1)[CH2:44][C@@H:43]([NH2:48])[CH2:42]2>CO>[Br:38][C:39]1[CH:40]=[C:41]2[C:45](=[CH:46][CH:47]=1)[CH2:44][C@@H:43]([NH2:48])[CH2:42]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 7915Isopropyl Acetate2×HCID 218580(1S)-(+)-Camphor-10-sulphonic acidHCID 86588388(r)-5-bromo-2-aminoindan (1S)-(+)-10-camphorsulfonate salt

Produkt 1

HCID 112758701H-Inden-2-amine, 5-bromo-2,3-dihydro-, (2R)-

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel5×

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

To the above solution is added 1300 mL of isopropyl acetate and 930 mL of methanol. The solution is stirred under nitrogen and heated to an internal temperature of 65° C. to achieve a gentle refluxing, over a period of 15 minutes. A solution of 103.1 g of (1S)-(+)-10-camphorsulfonic acid in 660 mL of methanol is added over a period of 15 minutes while maintaining an internal temperature of 60-65° C. to obtain a clear solution followed by 185 mL of methanol to achieve a v/v ratio of isopropyl acetate:methanol of about 2:1. The reaction mixture is cooled to 20-23° C. over a period of 2 hours. The mixture is stirred at room temperature (20-23° C.) for an additional 2 hours. The solid is collected, washed with 500 mL of precooled (to 0-2° C.) mixture of isopropyl acetate and methanol (2:1; v/v) in two equal portions of 250 mL each, and dried at 50-55° C. (100 mm Hg) to obtain crude (R)-5-bromo-2-aminoindane (1S)-(+)-10-camphorsulfonate salt as a white solid. A mixture of 90.0 g of crude (R)-5-bromo-2-aminoindane (1S)-(+)-10-camphorsulfonate salt and 900 mL of methanol is heated to a temperature of 65° C. to achieve a gentle refluxing. This suspension is stirred at 65° C. for 1 hour and the reaction mixture is cooled to 20-23° C. over a period of 2 hours and stirred at 20-23° C. for an additional 2 hours. The resulting solid is collected, washed with 190 mL of precooled (to 0-2° C.) mixture of isopropyl acetate and methanol (1:1; v/v) in two equal portions of 95 mL each. The solid is dried at 50-55° C. (100 mm Hg) to obtain (R)-5-bromo-2-aminoindane (1S)-(+)-10-camphosulfonate salt as a white solid (98.7% optical purity).

Aufarbeitung

  1. temperaturewhile maintaining an internal temperature of 60-65° C.
  2. customto obtain a clear solution
  3. temperatureThe reaction mixture is cooled to 20-23° C. over a period of 2 hours
  4. stirringThe mixture is stirred at room temperature (20-23° C.) for an additional 2 hours
  5. customThe solid is collected
  6. washwashed with 500 mL of precooled (to 0-2° C.) mixture of isopropyl acetate and methanol (2:1; v/v) in two equal portions of 250 mL each
  7. customdried at 50-55° C. (100 mm Hg)
  8. customto obtain crude (R)-5-bromo-2-aminoindane (1S)-(+)-10-camphorsulfonate salt as a white solid
  9. temperatureis heated to a temperature of 65° C.
  10. stirringThis suspension is stirred at 65° C. for 1 hour
  11. temperaturethe reaction mixture is cooled to 20-23° C. over a period of 2 hours
  12. stirringstirred at 20-23° C. for an additional 2 hours
  13. customThe resulting solid is collected
  14. washwashed with 190 mL of precooled (to 0-2° C.) mixture of isopropyl acetate and methanol (1:1; v/v) in two equal portions of 95 mL each
  15. customThe solid is dried at 50-55° C. (100 mm Hg)

Quellen und Nachweise

ORD-Eintrag
ord-5376e43697ce46e58461d0f1e611be1a
Quelldatensatz
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06878707B2

Notizen zur Reaktion

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