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

HRID 1016622Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1016622
[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

Komponenten

8

Edukt 6

HCID 313Hydrochloric AcidHCID 5238Sodium IodideHCID 71043-Hydroxy-2-naphthoic acidHCID 14798Sodium HydroxideHCID 24477Sodium ThiosulfateHCID 23665760Sodium Hypochlorite

Produkt 1

HCID 2422513-Hydroxy-4-iodonaphthalene-2-carboxylic acidAusbeute 75,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

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 6N 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): δ12.41(broad, 1 H), 8.63 (s,1 H), 8.05-7.97 (m, 2 H), 7.70 (m, 1 H), 7.42 (m, 1H).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-eeeb1e0c467d4d9bbffa589cc4737e20
Quelldatensatz
uspto-grants-2002_11
Patentnummer
US06476077B1

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