반응식
[OH:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([OH:12])[CH:8]=2)[CH:3]=1.[C:13](OC(=O)C)(=[O:15])[CH3:14].[C:20](O)(=[O:22])[CH3:21]>>[C:13]([O:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:12][C:20](=[O:22])[CH3:21])[CH:8]=2)[CH:3]=1)(=[O:15])[CH3:14]참가 물질
4
실험 절차
Thereafter, a mixture of 33.2 g (0.187 mole) of the thus obtained 2,6-dihydroxynaphthalene, 15.0 g of acetic acid and 44.9 g of acetic anhydride was stirred for 90 min in an oil bath kept at 140° C. After the reaction was over, the reaction mixture was cooled to room temperature and the thus precipitated crystals were collected by filtration, washed with acetic acid and dried to obtain 41.8 g of 2,6-diacetoxynaphthalene of white in color in a yield of 91.7%.
후처리
- customkept at 140° C
- filtrationthe thus precipitated crystals were collected by filtration
- washwashed with acetic acid
- customdried
출처 및 근거
- ORD 기록
- ord-a35b8b79b62442b49115615029a110fb
- 출처 데이터셋
- uspto-grants-1989_03
- 특허 번호
- US04814521
연결된 노트
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