Furfural → HCID 58860816, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=[O:10])=[CH:4][CH:3]=1.[O:12]1[CH:16]=[CH:15][CH:14]=[C:13]1[CH:17]=O.CCN(CC)CC.CC(OC(C)=O)=O>Cl>[Br:1][C:2]1[CH:3]=[CH:4][C:5](/[C:8](=[CH:17]\[C:13]2[O:12][CH:16]=[CH:15][CH:14]=2)/[C:9]([OH:11])=[O:10])=[CH:6][CH:7]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 140 °C
Procedure
A mixture of 4-bromophenylacetic acid (12.90 g, 60.0 mmol), 2-furancarboxaldehyde (6.0 mL, 72.0 mmol), NEt3 (12.0 mL, 86.4 mmol), and Ac2O (12.0 mL, 127.2 mmol) were heated at 140° C. (bath) with stirring for 1¾ h. The reaction mixture was cooled in an ice bath, before being treated with 2M HCl (30 mL) to adjust the pH to 1. A solid precipitated out of solution. This solid was extracted into Et2O (500 mL). The Et2O layer was washed with H2O (100 mL), before being extracted with 5% w/v aqueous Na2CO3 solution (5×100 mL). The aqueous extracts were washed with Et2O (2×50 mL), before being carefully acidified with AcOH to pH 6. The cream solid generated was collected, washed with H2O, and recrystallised from MeOH—H2O to give the title compound: m/z (ES+)=604.0 [2M+NH4]+.
Workup
- temperatureThe reaction mixture was cooled in an ice bath
- customA solid precipitated out of solution
- extractionThis solid was extracted into Et2O (500 mL)
- washThe Et2O layer was washed with H2O (100 mL)
- extractionbefore being extracted with 5% w/v aqueous Na2CO3 solution (5×100 mL)
- washThe aqueous extracts were washed with Et2O (2×50 mL)
- customThe cream solid generated was collected
- washwashed with H2O
- customrecrystallised from MeOH—H2O
Sources & evidence
- ORD record
- ord-aec9d51037f54432a9063be461128983
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07582632B2
Reaction notes
Loading…