Pyridine → HCID 85615786, compound
Reaction equation
[Br:1][CH2:2][C:3]([O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:4].[N:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>CC(C)=O>[Br-:1].[CH2:6]([O:5][C:3]([CH2:2][N+:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:4])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
To a solution of benzyl bromoacetate (10 g, 43.7 mmol) in acetone (200 mL) was added a solution of pyridine (3.51 mL, 43.7 mmol) in acetone (20 mL) and the resulting mixture was stirred at 60° C. under nitrogen over the week-end. Then allowed to cool to RT and concentrated to give the desired material. MS (LC/MS): 228.1 [MH]+.
Workup
- temperatureto cool to RT
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-9c6eeac9948e41bfac2e9a2d61ae7571
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09085555B2
Reaction notes
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