HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355375Generated: October 31, 2026
Hydrochloric Acid → 3-Hydroxy-4-iodonaphthalene-2-carboxylic acid
https://huagongshe.com/reaction/1355375
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 3-Hydroxy-2-naphthoic acid | HCID 7104 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Hydroxy-4-iodonaphthalene-2-carboxylic acid | HCID 242251 | 75.1% |
Reaction Steps
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, 1H), 8.63 (s, 1H), 8.05-7.97 (m, 2H), 7.70 (m, 1H), 7.42 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586432B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-91a03c6cba4449f78f2e6d7c1c1de93a |
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| Source note | uspto-grants-2003_07 |
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