Reaktion #1741840

ord-d1e87fdd38d5407da323612de74585ed

Reaktionsgleichung

[Na+].[OH-]
sodium hydroxide
C1=CC[C@H]2CNC[C@H]2C1
cis-3a,4,7,7a-tetrahydroisoindoline
BrCCc1ccc(Br)cc1
4-bromophenethyl bromide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Brc1ccc(CCN2C[C@H]3CC=CC[C@H]3C2)cc1
cis-2-(4-bromophenethyl)-3a,4,7,7a-tetrahydroisoindoline
Ausbeute 42.2%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheated in a 90° oil bath for 1 hour
  2. 2
    Extraktionthe aqueous layer was extracted with toluene
  3. 3
    workup.ADDITIONAddition of 10 mL of 10% hydrochloric acid to the toluene solution
  4. 4
    Sonstigeresulted in the formation of three layers
  5. 5
    ExtraktionExtraction with methylene chloride
  6. 6
    Sonstigegave 0.89 g of crude product which
  7. 7
    workup.DISTILLATIONon short-path distillation

Vorschrift

A mixture of 0.6 g of cis-3a,4,7,7a-tetrahydroisoindoline, 1.4 g of 4-bromophenethyl bromide, 1.0 g of potassium carbonate and 3 mL of dimethylformamide was stirred and heated in a 90° oil bath for 1 hour. Toluene (20 mL) and water (20 mL) were added and the aqueous layer was extracted with toluene. Addition of 10 mL of 10% hydrochloric acid to the toluene solution resulted in the formation of three layers. The two lower layers were made basic with aqueous sodium hydroxide solution. Extraction with methylene chloride gave 0.89 g of crude product which on short-path distillation gave 0.63 g of cis-2-(4-bromophenethyl)-3a,4,7,7a-tetrahydroisoindoline. 'H NMR (in CDCl3) δ7.4 (d, 2H); 7.0 (d, 2H); 5.8 (m, 2H); 3.0 (m, 2H); 2.6-2.8 (m, 4H); 2.4 (m, 2H); 2.1-2.3 (m, 4H) and 1.9 (d, 2H). The fumarate had m.p. 166°-167° after crystallization from ethanol. Anal. Calcd. for C20H24BrNO4 : C, 56.88; H, 5.73; N, 3.32 Found: C, 56.91; H, 5.64; N, 3.21

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05409929uspto-grants-1995_04