반응식
Br[C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([Cl:11])[CH:3]=1.[Cl:12][C:13]1[CH:14]=[CH:15][C:16]([O:22][CH3:23])=[C:17]([CH:21]=1)C(O)=O.C(=O)([O-])[O-].[Na+].[Na+].O1CCOCC1>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].CO>[Cl:11][C:4]1[CH:3]=[C:2]([C:15]2[CH:14]=[C:13]([Cl:12])[CH:21]=[CH:17][C:16]=2[O:22][CH3:23])[CH:10]=[CH:9][C:5]=1[C:6]([OH:8])=[O:7]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
4-bromo-2-chlorobenzoic acid (0.4 g), 5-chloro-2-methoxybenzoic acid (0.4 g), Pd(dppf)Cl2 (0.12 g), sodium carbonate (0.9 g), dioxan (15 ml) and methanol (5 ml) were charged to a flask and heated at reflux for 16 h. Cooled to room temp and filtered (hyflo). The filtrate was concentrated in vacuo, then dissolved in ethyl acetate. The suspension was made basic by addition of dilute NaOH. The aqueous layer was separated and acidified using 2M HCl, extracted with EtOAc, dried (MgSO4) and evaporated in vacuo to give the sub-title compound Yield 0.4 g
후처리
- temperatureheated
- temperatureat reflux for 16 h
- filtrationfiltered (hyflo)
- concentrationThe filtrate was concentrated in vacuo
- dissolutiondissolved in ethyl acetate
- additionThe suspension was made basic by addition of dilute NaOH
- customThe aqueous layer was separated
- extractionextracted with EtOAc
- dry with materialdried (MgSO4)
- customevaporated in vacuo
출처 및 근거
- ORD 기록
- ord-ab2b160fe763407f91689f6ef0679c8c
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07737135B2
연결된 노트
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