Potassium Cyanide → 2-(1-(Trifluoromethyl)cyclopropyl)acetonitrile
Reaction equation
CC1C=CC(S(O[CH2:12][C:13]2([C:16]([F:19])([F:18])[F:17])[CH2:15][CH2:14]2)(=O)=O)=CC=1.[C-:20]#[N:21].[K+]>CN(C=O)C>[F:19][C:16]([F:17])([F:18])[C:13]1([CH2:12][C:20]#[N:21])[CH2:14][CH2:15]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
Treat a solution of (1-(trifluoromethyl)cyclopropyl)methyl 4-methylbenzenesulfonate (12 g, 40.8 mmol) in DMF (150 mL) with potassium cyanide (3.5 g, 53 mmol) and heat at 50-70° C. for 3 days. Add water, extract with EtOAc (3×), wash the combined organics with water, then brine, dry and concentrate under reduced pressure to give the title compound (2.4 g, 39%). 1H NMR (400 MHz, CDCl3): δ 2.81 (s, 2H), 1.24-1.18 (m, 2H), 0.95-0.92 (m, 2H).
Workup
- extractionAdd water, extract with EtOAc (3×)
- washwash the combined organics with water
- dry with materialbrine, dry
- concentrationconcentrate under reduced pressure
Sources & evidence
- ORD record
- ord-c3bda80899534c15807f1241a4f107e6
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09187474B2
Reaction notes
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