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, 45 g of the thus obtained 2,6-dihydroxynaphthalene were acetylated with 23 g of acetic acid and 61 g of acetic anhydride in the same manner as in Example 7 to obtain 60.6 g of 2,6-diacetoxynaphthalene of the purity of 99.85% (by DSC) in a yield of 93.0%.
出典と根拠
- ORDレコード
- ord-125a9af4a1244cbc9c74452cd8c293f0
- 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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