Hydrochloric Acid → 3-Hydroxy-4-iodonaphthalene-2-carboxylic acid
반응식
[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]=2참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
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).
후처리
- stirringto stir for 30 min
- stirringstirring
- filtrationwas filtered
- washwashed with water (50 mL)
- customThe precipitate was transferred to a round-bottomed flask
- dissolutiondissolved in methanol (70 mL)
- concentrationtoluene (100 mL), concentrated
- dissolutionredissolved in methanol (70 mL)
- concentrationconcentrated
- dissolutionredissolved again in methanol (70 mL)
- concentrationtoluene (100 mL) and concentrated
출처 및 근거
- ORD 기록
- ord-91a468e8074240ae95dc74bd6ff3e694
- 출처 데이터셋
- uspto-grants-2005_06
- 특허 번호
- US06903092B2
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