Réaction #1121745

ord-b78177830a1643d3a4238b1c5d1e58e2

Équation de réaction

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
Rendement 94.8%

Solvants

Conditions de réaction

Température
150°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureAfter complete conversion, the reaction mixture was cooled to 25° C.
  2. 2
    Autreto layer separation
  3. 3
    LavageThe aqueous layer was washed once with 75 mL of methyl tert-butyl ether
  4. 4
    Lavagewashed once with 50 mL of water
  5. 5
    AutreThe combined organic layers were dried
  6. 6
    Autrethe volatiles were removed under reduced pressure

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08546112B2uspto-grants-2013_10