반응식
[C:1]([C:5]1[CH:11]=[C:10]([OH:12])[CH:9]=[CH:8][C:6]=1[OH:7])([CH3:4])([CH3:3])[CH3:2].Br[CH:14]([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[C:15]([O:17][CH2:18][CH3:19])=[O:16].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[OH:7][C:6]1[CH:8]=[CH:9][C:10]([O:12][CH:14]([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:11][C:5]=1[C:1]([CH3:4])([CH3:2])[CH3:3]참가 물질
5
실험 절차
116 g of tert-butylhydroquinone, 234 g of ethyl α-bromotetradecanoate and 170 g of potassium carbonate were mixed in 1.6 liters of acetone and reacted for 48 hours under refluxing and stirring. After the reaction, the acetone was distilled off and the residue was dissolved in one liter of ethyl acetate. The organic solvent layer was washed with water, dried with sodium sulfate and concentrated. The residue was recrystallized from 250 ml of n-hexane to obtain 110 g of a white solid. The melting point was 45° to 48° C.
후처리
- customreacted for 48 hours
- temperatureunder refluxing
- customAfter the reaction
- distillationthe acetone was distilled off
- dissolutionthe residue was dissolved in one liter of ethyl acetate
- washThe organic solvent layer was washed with water
- dry with materialdried with sodium sulfate
- concentrationconcentrated
- customThe residue was recrystallized from 250 ml of n-hexane
출처 및 근거
- ORD 기록
- ord-4c7b4f0e75604a328e7a60bee4c2460d
- 출처 데이터셋
- uspto-grants-1978_10
- 특허 번호
- US04120723
연결된 노트
불러오는 중…