StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Hydrochloric Acid → (S)-2-(1,4-Dibenzylpiperazin-2-yl)ethanol

HRID 131392
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 131392
[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][C@@H:9]1[CH:21]=[CH2:22])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C12BC(CCC1)CCC2.[OH-:32].[Na+].OO.Cl>O.CC(OC)(C)C.CCCCCCC.C1COCC1>[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][C@@H:9]1[CH2:21][CH2:22][OH:32])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 5

HCID 313Hydrochloric AcidHCID 784Hydrogen PeroxideHCID 14798Sodium Hydroxide2×HCID 789669-Borabicyclo(3.3.1)nonaneHCID 17759473(S)-1,4-dibenzyl-2-vinylpiperazine

Produkt 1

HCID 59732113(S)-2-(1,4-Dibenzylpiperazin-2-yl)ethanolAusbeute 99,1 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 962WaterLösungsmittel2×HCID 8028TetrahydrofuranLösungsmittel2×HCID 8900HeptaneLösungsmittelHCID 15413tert-Butyl methyl etherLösungsmittel2×

Versuchsvorschrift

Combine (S)-1,4-dibenzyl-2-vinyl-piperazine (131.0 g, 0.448 mol) and THF (500 mL) at ambient temperature. Add a 0.5M THF solution of 9-borabicyclo[3.3.1] nonane (9-BBN) (985.5 mL, 0.493 mol) over 20 minutes, keeping the pot temperature below 25° C. Stir the resulting mixture at ambient temperature for 16-18 hours. Cool the solution to 0-5° C. and quench with 3N NaOH (164.3 mL, 0.493 mol) over 5-10 minutes. Stir at 0-5° C. for 10-15 minutes and remove cooling bath. Add a 30% aqueous solution of hydrogen peroxide (160.2 mL, 1.57 mol) over 1 hour, maintaining a pot temperature of 30-35° C. Stir the resulting mixture for 1 hour and dilute with water (1.31 L) and MTBE (1.31 L). Layer separate and re-extract the aqueous layer with MTBE (655 mL). Combine organics and wash with water (2×655 mL) and brine (2×655 mL). Dry the MTBE solution over sodium sulfate, filter and concentrate in vacuo to afford 169.1 g of crude oil (theory=139.1 g). Treat the crude with 5N HCl (358 mL, 1.79 moles) and stir 5 minutes. Add water (250 mL) and stir 15-20 minutes. Add heptane (1.31 L) and stir 5 minutes. Layer separate and re-extract the aqueous layer with MTBE (655 mL). Discard these organic extracts and add 5N NaOH (403 mL, 2.02 moles) to the aqueous portion. Stir 5 minutes then dilute with MTBE (1.31 L) and layer separate. Re-extract the aqueous layer with MTBE (655 mL). Combine the MTBE extracts and wash with water (655 mL), then dry over sodium sulfate, filter and concentrate in vacuo to afford 137.8 g (99.0%) of the title compound. 1H NMR (500 MHz, DMSO-d6) δ 1.87 (m, 1H), 2.03 (m, 1H), 2.33 (m, 2H), 2.43 (m, 1H), 2.50 (d, 1H), 2.66 (d, 1H), 2.83 (m, 1H), 2.93 (m, 1H), 3.39 (d, 1H), 3.50 (m, 1H), 3.74 (m, 1H), 3.88 (m, 1H), 4.18 (d, 1H), 4.80 (bs, 1H), 7.26 (m,2H), 7.32 (m, 8H).

Aufarbeitung

  1. customat ambient temperature
  2. customthe pot temperature below 25° C
  3. temperatureCool the solution to 0-5° C.
  4. stirringStir at 0-5° C. for 10-15 minutes
  5. customremove
  6. temperaturecooling bath
  7. temperaturemaintaining a pot temperature of 30-35° C
  8. stirringStir the resulting mixture for 1 hour
  9. customLayer separate
  10. extractionre-extract the aqueous layer with MTBE (655 mL)
  11. washCombine organics and wash with water (2×655 mL) and brine (2×655 mL)
  12. dry with materialDry the MTBE solution over sodium sulfate
  13. filtrationfilter
  14. concentrationconcentrate in vacuo
  15. customto afford 169.1 g of crude oil (theory=139.1 g)
  16. stirringstir 5 minutes
  17. customLayer separate
  18. extractionre-extract the aqueous layer with MTBE (655 mL)
  19. stirringStir 5 minutes
  20. customseparate
  21. washCombine the MTBE extracts and wash with water (655 mL)
  22. dry with materialdry over sodium sulfate
  23. filtrationfilter
  24. concentrationconcentrate in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-ccbf88967ae942c5ae3a3f290cf2795d
Quelldatensatz
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07384934B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion