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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415671Generated: October 30, 2026

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

https://huagongshe.com/reaction/2415671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
Reactant3-Hydroxy-2-naphthoic acidHCID 7104—
ReactantSodium HydroxideHCID 14798—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium HypochloriteHCID 23665760—
SolventMethanolHCID 887—
Product3-Hydroxy-4-iodonaphthalene-2-carboxylic acidHCID 24225175.1%

Reaction Conditions

Temperature0 °C

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): δ 12.41 (broad, 1 H), 8.63 (s, 1 H), 8.05-7.97 (m, 2 H), 7.70 (m, 1 H), 7.42 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821973B2
Source datasetuspto-grants-2004_11
ORD IDord-7aea32cdf3f44fe28822c5dfac0356a4
Source noteuspto-grants-2004_11