Dimethylformamide → 2-Fluoro-6-(prop-1-yn-1-yl)benzaldehyde
Reaction equation
Br[C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[CH:4]=[O:5].C(N([CH2:16][CH3:17])CC)C.[CH3:18]N(C)C=O>Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Cu]I>[F:10][C:6]1[CH:7]=[CH:8][CH:9]=[C:2]([C:18]#[C:16][CH3:17])[C:3]=1[CH:4]=[O:5]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- -78 °C
Procedure
A mixture of 2-bromo-6-fluorobenzaldehyde [see Tetrahedron Letters (1992), 33(49), 7499-7502] (4.0 g; 19.7 mmol) and triethylamine (4.12 ml; 29.5 mmol) in anhydrous N,N-dimethylformamide (75 ml) contained within a large (200 ml capacity) sealed tube was cooled to −78° C. and propyne gas bubbled through until the volume had increased by approx 10 ml. To this mixture was added Pd(PPh3)2Cl2 (0.69 g; 0.99 mmol) and CuI (180 mg; 1.97 mmol), the lid was put in place and the tube allowed to reach room temperature and stir for 4 hours after which TLC showed the reaction was complete. The mixture was poured onto water (500 ml) and extracted with EtOAc (3×150 ml). The combined EtOAc layers were washed with water (3×400 ml), saturated NaCl (150 ml), dried over Na2SO4, filtered through a 1 inch plug of silica and evaporated to give the title compound (3.2 g, 100%).
Workup
- customsealed tube
- custompropyne gas bubbled through until the volume
- temperaturehad increased by approx 10 ml
- customto reach room temperature
- additionThe mixture was poured onto water (500 ml)
- extractionextracted with EtOAc (3×150 ml)
- washThe combined EtOAc layers were washed with water (3×400 ml), saturated NaCl (150 ml)
- dry with materialdried over Na2SO4
- filtrationfiltered through a 1 inch plug of silica
- customevaporated
Sources & evidence
- ORD record
- ord-b39789b4454e485c9afecd188cf4ceee
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285563B2
Reaction notes
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