Methanol → 2-(3',4'-Dihydroxybenzyl)-5-(2-phenylethyl) pyrrolidine hydrobromide

HRID 256202Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 256202
C[O:2][C:3]1[CH:4]=[C:5]([CH:20]=[CH:21][C:22]=1[O:23]C)[CH2:6][CH:7]1[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[NH:8]1.B(Br)(Br)[Br:26].CO>C(Cl)Cl>[BrH:26].[OH:2][C:3]1[CH:4]=[C:5]([CH:20]=[CH:21][C:22]=1[OH:23])[CH2:6][CH:7]1[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[NH:8]1

Komponenten

5

Edukt 3

HCID 887MethanolHCID 25134Boron tribromideHCID 130650362-(3'4'-Dimethoxybenzyl)-5-(2-phenylethyl)pyrrolidine

Produkt 1

HCID 130650372-(3',4'-Dihydroxybenzyl)-5-(2-phenylethyl) pyrrolidine hydrobromide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a cold (-70° C.) solution of 15.1 g (0.057 mole) of 2-(3'4'-dimethoxybenzyl)-5-(2-phenylethyl)pyrrolidine in 1 L of methylene chloride was added dropwise 55.1 g (0.22 mole) of boron tribromide. After the addition the reaction mixture was gradually warmed up to room temperature over a period of 2 h. The mixture was cooled again to -70° C. and 300 ml. of methanol was carefully added. Solvent was removed in vacuo. An additional 100 ml of methanol was added and removed in vacuo. The gummy dark residue was boiled in ethyl acetate and decanted, then triturated with ethyl acetate and left overnight to give a solid. This was recrystallized twice from acetonitrile to give 6 g. m.p. 149°-151° C.

Aufarbeitung

  1. additionAfter the addition the reaction mixture
  2. temperatureThe mixture was cooled again to -70° C.
  3. customSolvent was removed in vacuo
  4. additionAn additional 100 ml of methanol was added
  5. customremoved in vacuo
  6. customdecanted
  7. customtriturated with ethyl acetate
  8. customto give a solid
  9. customThis was recrystallized twice from acetonitrile
  10. customto give 6 g

Quellen und Nachweise

ORD-Eintrag
ord-2169a1109d5c4e08a3ade7d3c02f1ef8
Quelldatensatz
uspto-grants-1987_10
Patentnummer
US04701461

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