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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590666Generated: November 3, 2026

Hydrochloric Acid → HCID 19767967, compound

https://huagongshe.com/reaction/1590666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantMethyl iodideHCID 6328—
ReactantMagnesiumHCID 5462224—
ReactantHCID 21623532HCID 21623532—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19767967HCID 1976796773%

Reaction Steps

To a suspension of anhydrous magnesium (0.23 g) and a small crystal of iodine in anhydrous diethyl ether (3 ml) a solution of methyl iodide (1.3 g) in anhydrous diethyl ether (6 ml) is added dropwise. The mixture is refluxed for 1 hour then cooled to room temperature. To this mixture a solution of tert-butyl 5,6,7,8-tetrahydro-7-(1H-imidazol-1-ylmethyl)-8-oxo-2-naphthalenecaboxylate (1.0 g) in anhydrous tetrahydrofuran (25 ml) is added dropwise. The reaction mixture, after stirring at room temperature for 2 hours, is poured into water, neutralized with diluited hydrochloric acid and extracted with methylene chloride. The organic layer is dried over sodium sulfate and evaporated to dryness. The residue is taken up with trifluoracetic acid and refluxed for 45 minutes. The resulting solution is evaporated under reduced pressure and the residue is purified by silica gel column chromatography, eluiting with methylene chloride-methanol-acetic acid (180:20:2), to give 0.6 g of 5,6-dihydro-7-(1H-imidazol-1-ylmethyl)-8-methyl-2-naphthalenecarboxylic acid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05204364
Source datasetuspto-grants-1993_04
ORD IDord-2c99163a4bc74273b431d7c92c4a77a4
Source noteuspto-grants-1993_04