Reaktion #1121745

ord-b78177830a1643d3a4238b1c5d1e58e2

Reaktionsgleichung

COC(C)(C)C
methyl tert-butyl ether
O
Water
[Cl-].[Na+]
NaCl
CCOC(=O)C(C(=O)OCC)C(CC(C)C)C[N+](=O)[O-]
2-(3-methyl-1-nitromethyl-butyl)-malonic acid diethyl ester
O
water
CCOC(=O)CC(CC(C)C)C[N+](=O)[O-]
5-methyl-3-nitromethyl-hexanoic acid ethyl ester
Ausbeute 94.8%

Lösungsmittel

Reaktionsbedingungen

Temperatur
150°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter complete conversion, the reaction mixture was cooled to 25° C.
  2. 2
    Sonstigeto layer separation
  3. 3
    WaschenThe aqueous layer was washed once with 75 mL of methyl tert-butyl ether
  4. 4
    Waschenwashed once with 50 mL of water
  5. 5
    SonstigeThe combined organic layers were dried
  6. 6
    Sonstigethe volatiles were removed under reduced pressure

Vorschrift

10.0 g (34 mmol) of 2-(3-methyl-1-nitromethyl-butyl)-malonic acid diethyl ester (XII, R1=ethyl) were dissolved in 140 mL of DMSO. Water (10.4 mL) and solid NaCl (14.6 g) were added and the mixture was heated for 6 hours at 150° C. After complete conversion, the reaction mixture was cooled to 25° C. and 150 mL of methyl tert-butyl ether were added. 100 mL of water were added slowly. The heterogeneous mixture was stirred for 5 minutes prior to layer separation. The aqueous layer was washed once with 75 mL of methyl tert-butyl ether. The organic layers were combined and washed once with 50 mL of water. The combined organic layers were dried and the volatiles were removed under reduced pressure to give 7.0 g of 5-methyl-3-nitromethyl-hexanoic acid ethyl ester (VIII, R1=ethyl; 93% yield).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08546112B2uspto-grants-2013_10