반응식
[C:1]1([C:11]2[CH:16]=[CH:15][C:14]([C:17](OC)=[O:18])=[CH:13][CH:12]=2)[CH:6]=[CH:5][C:4]([C:7](OC)=[O:8])=[CH:3][CH:2]=1.C1COCC1.O>C(Cl)Cl>[C:11]1([C:1]2[CH:6]=[CH:5][C:4]([CH:7]=[O:8])=[CH:3][CH:2]=2)[CH:16]=[CH:15][C:14]([CH:17]=[O:18])=[CH:13][CH:12]=1참가 물질
실험 절차
Next, 27.1 g (0.10 mole) of dimethyl 4,4′-biphenyldicarboxylate and 133.4 g of THF were introduced to a 2000-ml four-necked reaction vessel. To this solution was added the reagent solution prepared above in drops at 5° C. or below. After the dropwise addition, stirring was continued at 15° C. for 4.5 hours. Upon completion of the reaction, extraction was performed by adding in drops 622.2 g of methylene chloride and 411.2 g of water. The methylene chloride layer obtained was concentrated until dryness under reduced pressure. The residue was dissolved in acetone by adding 303.2 g of acetone in drops and then 1600.3 g of water was added in drops at 20° C. Thereafter, the mixture was stirred day and night at 5° C. and a solid was recovered by filtration. The solid thus obtained was washed with acetone and dried under reduced pressure to give 18.1 g of 4,4′-biphenyldicarboxaldehyde.
후처리
- additionTo this solution was added the reagent solution
- customprepared above in drops at 5° C. or below
- additionAfter the dropwise addition
- customUpon completion of the reaction, extraction
- concentrationwas concentrated until dryness under reduced pressure
- dissolutionThe residue was dissolved in acetone
- additionby adding 303.2 g of acetone in drops
- addition1600.3 g of water was added in drops at 20° C
- stirringThereafter, the mixture was stirred day and night at 5° C.
- filtrationa solid was recovered by filtration
- customThe solid thus obtained
- washwas washed with acetone
- customdried under reduced pressure
출처 및 근거
- ORD 기록
- ord-25c872cf8d544280ace618887109e235
- 출처 데이터셋
- uspto-grants-2009_09
- 특허 번호
- US07582364B2
연결된 노트
불러오는 중…