Ethyl bromoacetate → Ethyl 5-Acetoxy-7-(2,4-dichlorophenyl)-3-hydroxy-3-methyl-6-heptenoate

HRID 354573Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 354573
[C:1]([O:4][CH:5]([CH:10]=[CH:11][C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[Cl:19])[CH2:6][C:7](=[O:9])[CH3:8])(=[O:3])[CH3:2].BrC[C:22]([O:24][CH2:25][CH3:26])=[O:23].[Cl-].[CH2:28]([Al+]CC)C>C1COCC1.[Zn]>[C:1]([O:4][CH:5]([CH:10]=[CH:11][C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[Cl:19])[CH2:6][C:7]([OH:9])([CH3:28])[CH2:8][C:22]([O:24][CH2:25][CH3:26])=[O:23])(=[O:3])[CH3:2]

Komponenten

6

Versuchsvorschrift

A solution of 6-(2,4-dichlorophenyl)-2-oxo-5-hexene-4-yl acetate (1.3 g, 4.3 mmole) and ethyl bromoacetate (0.47 ml, 4.2 mmole) in dry THF (10 ml) was added dropwise to a vigorously stirred slurry of activated zinc dust (490 mg, 7.5 mmole), cuprous bromide (29 mg, 0.2 mmole), diethylaluminum chloride (25% solution in toluene; 1.72 ml, 4.3 mmole) and dry THF (5 ml) under N2 at 20° C. Stirring was continued for 5 hours before quenching with pyridine (3.5 ml). After the addition of water (50 ml) the mixture was extracted with ether (3×80 ml). The combined ether extracts were washed with 1 N HCl (2×25 ml), H2O (2×50 ml) and brine, then dried (MgSO4), filtered and evaporated leaving the crude title compound as a pale yellow oil (1.2 g); pmr (CDCl3) δ1.28 (3 H, t), 1.33 (3H, t), 2.10 (3H, s).

Aufarbeitung

  1. custombefore quenching with pyridine (3.5 ml)
  2. additionAfter the addition of water (50 ml) the mixture
  3. extractionwas extracted with ether (3×80 ml)
  4. washThe combined ether extracts were washed with 1 N HCl (2×25 ml), H2O (2×50 ml) and brine
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-70e71b7d612e41a19000ff3c86dc976e
Quelldatensatz
uspto-grants-1983_03
Patentnummer
US04375475

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