Water → HCID 131725687, compound
Reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[C-]#N.[K+].[N:13]1C(C)=CC=C[C:14]=1C.O.[C:22]([O:25]C(=O)C)(=[O:24])[CH3:23]>C(Cl)Cl.[V]>[C:22]([OH:25])(=[O:24])[CH3:23].[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]([OH:5])[C:14]#[N:13]Participants
Procedure
o-Chlorobenzaldehyde (2.0 g, 1.62 ml, 14.23 mmol) was added via syringe to an agitated mixture of potassium cyanide (2.793 g, 43.8 mmol) and a vanadium catalyst* of Formula (7) (90 mg, 14.23×10−2 mmol) in CH2Cl2 (55 ml), followed by 2,6-lutidine (0.147 g, 0.16 ml, 1.37 mmol) and water (0.25 g, 0.25 ml, 13.66 mmol). The slurry was cooled to a temperature of −6° C. and acetic anhydride (3.08 g, 2.85 ml, 30.17 mmol) was added via a syringe. The slurry was agitated at a temperature of −5° C. to 0° C. Analysis by G.C. showed that the reaction had gone to 51% conversion (62% e.e.) after 4 hrs and to 61% conversion (53% e.e.) after 7 hrs. The excess potassium cyanide was filtered off and the product was washed with dichloromethane before the filtrates were reduced in vacuo. The residues were dissolved in 10:2 v/v hexane:ethyl acetate and the catalyst was removed by passing the mixture through a bed of silica and washing with 10:1 v/v hexane:ethyl acetate.
Workup
- additionwas added via a syringe
- filtrationThe excess potassium cyanide was filtered off
- washthe product was washed with dichloromethane before the filtrates
- dissolutionThe residues were dissolved in 10:2 v/v hexane
- customethyl acetate and the catalyst was removed
- washwashing with 10:1 v/v hexane
Sources & evidence
- ORD record
- ord-867ac05b96c142c9a491d3ff4f48a87c
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07022876B2
Reaction notes
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