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Hydrochloric Acid → Methyl 4-(4-fluorobenzyl)-3-methoxycarbonylbenzoate

HRID 2187620
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2187620
[Br-].[F:2][C:3]1[CH:10]=[CH:9][C:6]([CH2:7][Zn+])=[CH:5][CH:4]=1.Br[C:12]1[CH:21]=[CH:20][C:15]([C:16]([O:18][CH3:19])=[O:17])=[CH:14][C:13]=1[C:22]([O:24][CH3:25])=[O:23].Cl>O1CCCC1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd]>[F:2][C:3]1[CH:10]=[CH:9][C:6]([CH2:7][C:20]2[CH:21]=[CH:12][C:13]([C:22]([O:24][CH3:25])=[O:23])=[CH:14][C:15]=2[C:16]([O:18][CH3:19])=[O:17])=[CH:5][CH:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 2824912Dimethyl 4-bromoisophthalateHCID 178505763HCID 178505763, Verbindung

Produkt 1

HCID 18476032Methyl 4-(4-fluorobenzyl)-3-methoxycarbonylbenzoate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6505921(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumKatalysator
HCID 8028
Tetrahydrofuran
Lösungsmittel
2×

Versuchsvorschrift

A 2.OM solution of 4-fluorobenzyl zinc bromide in tetrahydrofuran (95 ml, 190 mmol; Negishi, E-i. and King, A. O., J.O.C.1977,42,1821) was added dropwise over 20 minutes to a stirred solution of dimethyl 4-bromoisophthalate (20.0 g, 73.2 mmol) and tris(dibenzylideneacetone)dipalladium(O) (0.67 g,0.73 mmol) in tetrahydrofuran (270 ml) at ambient temperature under an inert atmosphere. During the addition the internal temperature rose to 40° C. The reaction mixture was stirred for 3 hours and then poured into 2M. HCl (1500 ml), cooled in an ice bath and the product extracted into ethyl acetate (3×700 ml). The extracts were washed with water (500 ml), brine (500 ml), dried, and the solvent evaporated under reduced pressure. The residue was taken up in a small quantity of dichloromethane, isohexane added, and the solid which crystallised from the solution, filtered and dried to give methyl 4-(4-fluorobenzyl)-3-methoxycarbonylbenzoate (10.5 g)

Aufarbeitung

  1. additionDuring the addition the internal temperature
  2. customrose to 40° C
  3. additionpoured into 2M
  4. extractionthe product extracted into ethyl acetate (3×700 ml)
  5. washThe extracts were washed with water (500 ml), brine (500 ml)
  6. customdried
  7. customthe solvent evaporated under reduced pressure
  8. additionadded
  9. customthe solid which crystallised from the solution
  10. filtrationfiltered
  11. customdried

Quellen und Nachweise

ORD-Eintrag
ord-a735db8a0cd6486a8bab4dd3323ed27f
Quelldatensatz
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06410539B1

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