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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550234Generated: October 30, 2026

Ammonium Chloride → (4-Bromo-naphthalen-2-yl)-(5-fluorobenzo[b]-thiophen-2-yl)methanol

https://huagongshe.com/reaction/550234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Fluoro-1-benzothiopheneHCID 11815950—
Reactant4-Bromonaphthalene-2-carbaldehydeHCID 54338128—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-naphthalen-2-yl)-(5-fluorobenzo[b]-thiophen-2-yl)methanolHCID 6715671269%

Reaction Steps

In a nitrogen stream, an n-butyllithium hexane solution (1.6 M, 1.68 ml, 2.68 mmol) was added dropwise to a solution of 5-fluorobenzo[b]thiophene (410 mg, 2.68 mmol) in THF (10 ml) and the reaction solution was stirred at the same temperature for 10 minutes. To this solution, a solution of 4-bromonaphthalene-2-carbaldehyde (600 mg, 2.55 mmol) in THF (5 ml) was added dropwise at −78° C. The obtained mixture was stirred at the same temperature for two hours, and then a saturated ammonium chloride aqueous solution was added and the mixture was extracted with ether. The organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous magnesium sulfate), and then the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:10)] to obtain the title compound (680 mg, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943748B2
Source datasetuspto-grants-2011_05
ORD IDord-429b452d47d14a6bb4f5faa5936325fb
Source noteuspto-grants-2011_05