4-Bromo-2-fluorobenzaldehyde → 4-Bromo-1-ethenyl-2-fluorobenzene
반응식
[CH2:1]([Li])CCC.[Br:6][C:7]1[CH:14]=[CH:13][C:10]([CH:11]=O)=[C:9]([F:15])[CH:8]=1>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O1CCCC1>[Br:6][C:7]1[CH:14]=[CH:13][C:10]([CH:11]=[CH2:1])=[C:9]([F:15])[CH:8]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
To a suspension of methyltriphenylphosphonium bromide (1.1 eq) in tetrahydrofuran (0.13M) at −78° C., was added n-butyllithium (2.5M in hexanes, 1.1 eq) dropwise over 20 min. The reaction mixture was stirred at −78° C. for 15 min, warm to 0° C., stirred for 15 min and cooled back to −78° C. A solution of 4-bromo-2-fluoro-benzaldehyde (1 eq) in 100 mL THF was added dropwise over 30 min. Final mixture was allowed to warm slowly to rt and stirred for 1 h. The resulting mixture was quenched with a saturated NH4Cl solution and diluted with 2 volume of hexane. The organic extract was washed with brine, dried over MgSO4, filtered and concentrated. The residue was diluted with Hexane/EtOAc (9:1) and filtered on a pad of Silica gel. The fractions were combined and concentrated to afford the desired material.
후처리
- temperaturewarm to 0° C.
- stirringstirred for 15 min
- temperaturecooled back to −78° C
- temperatureto warm slowly to rt
- stirringstirred for 1 h
- customThe resulting mixture was quenched with a saturated NH4Cl solution
- additiondiluted with 2 volume of hexane
- extractionThe organic extract
- washwas washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- additionThe residue was diluted with Hexane/EtOAc (9:1)
- filtrationfiltered on a pad of Silica gel
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-0870938f9cd94aab96f8266dc374c8d5
- 출처 데이터셋
- uspto-grants-2007_07
- 특허 번호
- US07238706B2
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