反応式
[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]参加物
4
実験手順
Subsequently, 6.0 g (0.035 mol) of the thus obtained 2,6-dihydroxynaphthalene were acetylated with 2.7 g of acetic acid and 7.9 g of acetic anhydride in the same manner as in Example 7 to obtain 7.9 g of 2,6-diacetoxynaphthalene of white in color in a yield of 92.5%.
出典と根拠
- ORDレコード
- ord-d8d55be284db4bcd853ca653224dc49d
- 出典データセット
- uspto-grants-1989_03
- 特許番号
- US04814521
関連ノート
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