반응식
[CH3:1][CH:2]([C:4]1[CH2:13][CH2:12][C@H:11]2[C:6](=[CH:7][CH2:8][C@H:9]3[C@@:17]([C:19]([OH:21])=[O:20])([CH3:18])[CH2:16][CH2:15][CH2:14][C@@:10]32[CH3:22])[CH:5]=1)[CH3:3].CO.C(O)C.C(O)=CC>[Pd].C1C=CC=CC=1.C(O)(=O)C>[CH3:3][CH:2]([C:4]1[CH:13]=[CH:12][C:11]2[C@@:10]3([CH3:22])[CH2:14][CH2:15][CH2:16][C@:17]([C:19]([OH:21])=[O:20])([CH3:18])[C@@H:9]3[CH2:8][CH2:7][C:6]=2[CH:5]=1)[CH3:1]참가 물질
8
실험 절차
said abietic acid at 200–300° C. for 1–5 hours with the catalyst of 0.1–5% (wt) of 5%–10% palladium/carbon, or incubating directly at 220–380° C. After incubation and cooling down, adding 0.5 to 10-fold (volume) solvent, said solvent can be any one of methanol, ethanol, propenol, acetyester acetic acid, benzene and methbenzene, keeping refluxed for 1–3 hours, filtering when it is warm, cooling down, allowing it to stand for overnight and be crystallized. Dehydroabietic acid is obtained after filtering.
후처리
- customat 200–300° C.
- customfor 1–5 hours
- customincubating directly at 220–380° C
- temperatureAfter incubation and cooling down
- additionadding 0.5 to 10-fold (volume) solvent
- temperaturekeeping refluxed for 1–3 hours
- filtrationfiltering when it
- temperatureis warm
- temperaturecooling down
- custombe crystallized
출처 및 근거
- ORD 기록
- ord-a674de46ce834a52b48eb19e4e6e755e
- 출처 데이터셋
- uspto-grants-2006_03
- 특허 번호
- US07015343B2
연결된 노트
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