반응식
[CH3:1][C:2]1([CH3:17])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]2[CH:7]=[C:6]([C:14](Cl)=[O:15])[CH:5]=[CH:4][C:3]1=2.Br[CH2:19][C:20]1[CH:29]=[CH:28][C:23]([C:24]([O:26][CH3:27])=[O:25])=[CH:22][CH:21]=1>C(COC)OC.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.[Zn]>[C:24]([C:23]1[CH:28]=[CH:29][C:20]([CH2:19][C:14]([C:6]2[CH:5]=[CH:4][C:3]3[C:2]([CH3:17])([CH3:1])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]=3[CH:7]=2)=[O:15])=[CH:21][CH:22]=1)([O:26][CH3:27])=[O:25]참가 물질
6
반응물 2
생성물 1
시약·촉매·용매 3
실험 절차
A solution of 4 g (16 mmol) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalene-2-carbonyl chloride and 4 g (16 mmol) of methyl 4-bromomethylbenzoate in 20 ml of dimethoxyethane was added dropwise to a solution or suspension of 0.56 g of bis(triphenylphosphine)palladium(II) dichloride and 2.1 g of zinc powder in 40 ml of dimethoxyethane at room temperature. The reaction mixture was then refluxed for 6 h. After cooling, solids were filtered off and the filtrate was heated with active carbon and filtered hot. The filtrate was concentrated and yielded after recrystallization 3× from methanol and finally from isopropanol 0.9 g of the title compound of melting point 103°-104° C.
후처리
- temperatureThe reaction mixture was then refluxed for 6 h
- temperatureAfter cooling
- filtrationsolids were filtered off
- temperaturethe filtrate was heated with active carbon
- filtrationfiltered hot
- concentrationThe filtrate was concentrated
- customyielded
- customafter recrystallization 3× from methanol
출처 및 근거
- ORD 기록
- ord-559cf94ba15743f9b524eafb19affb8b
- 출처 데이터셋
- uspto-grants-1993_03
- 특허 번호
- US05194664
연결된 노트
불러오는 중…