Hydrochloric Acid → 3-Hydroxy-4-iodonaphthalene-2-carboxylic acid

HRID 1070448ノート

反応式

HRID 1070448 の反応式
[OH-].[Na+].[I-:3].[Na+].[OH:5][C:6]1[C:7]([C:16]([OH:18])=[O:17])=[CH:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[CH:11][CH:10]=2.Cl[O-].[Na+].S([O-])([O-])(=O)=S.[Na+].[Na+].Cl>CO>[OH:5][C:6]1[C:7]([C:16]([OH:18])=[O:17])=[CH:8][C:9]2[C:14]([C:15]=1[I:3])=[CH:13][CH:12]=[CH:11][CH:10]=2

参加物

8

反応条件

温度
0 °C

実験手順

A mixture of NaOH (2.12 g) in methanol (100 mL) was stirred until the solution was homogeneous. Sodium iodide (3.98 g) and 3-hydroxy-2-naphthoic acid (5.00 g) were added and allowed to stir for 30 min. The resulting suspension was cooled to 0° C. and a 5.25% (w/v) aqueous solution of sodium hypochlorite was added dropwise and stirring continued for 1 h. Saturated sodium thiosulfate (25 mL) was added and after 5 min the solution was acidified to pH 2 by addition of 6 N HCl resulting in the formation of a yellow precipitate which was filtered and washed with water (50 mL). The precipitate was transferred to a round-bottomed flask, dissolved in methanol (70 mL) and toluene (100 mL), concentrated, redissolved in methanol (70 mL), concentrated, redissolved again in methanol (70 mL) and toluene (100 mL) and concentrated to afford the product as a yellow solid (6.26 g). MS m/z 313 (M−1). 1H NMR (DMSO-d6): δ 12.41 (broad, 1H), 8.63 (s, 1H), 8.05-7.97 (m, 2H), 7.70 (m, 1H), 7.42 (m, 1H).

後処理

  1. stirringto stir for 30 min
  2. stirringstirring
  3. filtrationwas filtered
  4. washwashed with water (50 mL)
  5. customThe precipitate was transferred to a round-bottomed flask
  6. dissolutiondissolved in methanol (70 mL)
  7. concentrationtoluene (100 mL), concentrated
  8. dissolutionredissolved in methanol (70 mL)
  9. concentrationconcentrated
  10. dissolutionredissolved again in methanol (70 mL)
  11. concentrationtoluene (100 mL) and concentrated

出典と根拠

ORDレコード
ord-91a468e8074240ae95dc74bd6ff3e694
出典データセット
uspto-grants-2005_06
特許番号
US06903092B2

反応ノート

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