Diethyl Ether → 2-Cyano-2-methyl-propanoic acid methyl ester
Reaction equation
CO[C:3](=O)[CH2:4][C:5]#N.[C:8]([O-:11])([O-])=[O:9].[Cs+].[Cs+].CI.[CH3:16]COCC.C[N:22]([CH:24]=O)C>[Cl-].[Na+].O>[CH3:16][O:11][C:8](=[O:9])[C:4]([C:24]#[N:22])([CH3:5])[CH3:3]Participants
7
Procedure
A mixture of cyano-acetic acid methyl ester (11 g, 111 mmol), Cs2CO3 (108 g, 333 mmol) and methyl iodide (35 mL, 556 mmol) in anhydrous DMF (300 mL) was stirred at r.t. for 3 days. Brine (100 mL) and ether (250 mL) were added, and the aqueous layer was extracted with additional ether (250 mL). The organic layers were combined, washed with water (4×200 mL), and dried over MgSO4. The solvent was evaporated to give 11 g of the title compound as a yellow oil. 1H NMR (CDCl3, 200 MHz): δ ppm=3.83 (s, 3H), 1.63 (s, 6H).
Workup
- extractionthe aqueous layer was extracted with additional ether (250 mL)
- washwashed with water (4×200 mL)
- dry with materialdried over MgSO4
- customThe solvent was evaporated
Sources & evidence
- ORD record
- ord-17d5b548ea6a48988478639a7fb53c25
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409892B2
Reaction notes
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