Carbon Dioxide → 6-Hydroxy-2-naphthoic acid

HRID 67193

反応式

HRID 67193 の反応式
[OH:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=1.[OH-].[K+].[C:14](=O)([O-:16])[O-:15].[K+].[K+].[C:20](=[O:22])=[O:21]>>[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([C:14]([OH:16])=[O:15])[CH:6]=[CH:5]2.[OH:1][C:2]1[C:11]([C:20]([OH:22])=[O:21])=[CH:10][C:9]2[C:4]([CH:3]=1)=[CH:5][CH:6]=[CH:7][CH:8]=2

参加物

6

反応物 4

HCID 280Carbon DioxideHCID 86632-NaphtholHCID 11430Potassium CarbonateHCID 14797Potassium Hydroxide

生成物 2

HCID 71043-Hydroxy-2-naphthoic acidHCID 855576-Hydroxy-2-naphthoic acid収率 48.1%

実験手順

The procedure of Example 1 is followed in every detail except that a mixture of 2-hydroxynaphthalene (83 grams; 0.576 mole), 45% potassium hydroxide (69.7 grams; 0.559 mole), and potassium carbonate (20 grams; 0.145 mole) is employed initially, the dehydrated reaction mixture is heated under 60 psi of carbon dioxide for 10 hours, and the aqueous phase is washed twice with 100-ml portions of isopropylnaphthalene at 85°-95° C. There is obtained 25.5 grams of 6-hydroxy-2-naphthoic acid (48.1% of theoretical), and 4.6 grams of 3-hydroxy-2-naphthoic acid.

後処理

  1. washthe aqueous phase is washed twice with 100-ml portions of isopropylnaphthalene at 85°-95° C

出典と根拠

ORDレコード
ord-4dfb55a228b64a9aaa64bd694a289a5f
出典データセット
uspto-grants-1982_08
特許番号
US04345094

関連ノート

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