反应 #1121745

ord-b78177830a1643d3a4238b1c5d1e58e2

反应方程式

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
收率 94.8%

溶剂

反应条件

温度
150°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

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

实验过程

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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08546112B2uspto-grants-2013_10