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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988796Generated: October 25, 2026

Pyridine → {[1-(naphthalen-1-yl)-1H-tetrazol-5-yl]sulfanyl}acetic acid

https://huagongshe.com/reaction/1988796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl bromoacetateHCID 60984—
Reactant1,2-Dihydro-1-naphthyl-5H-tetrazole-5-thioneHCID 2731701—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product{[1-(naphthalen-1-yl)-1H-tetrazol-5-yl]sulfanyl}acetic acidHCID 2907025992.3%

Reaction Steps

Pyridine (0.83 mL, 10.3 mmol) and 1,2-dihydro-1-(1-naphthalenyl)-5H-tetrazole-5-thione (2.14 g, 9.38 mmol) were added to a solution of methyl 2-bromoacetate (977 μL, 10.3 mmol) in DMSO (50 mL). The resulting light yellow solution was stirred at room temperature for 2 h. The reaction mixture was then diluted with EtOAc (300 ml) and was successively washed with water (2×250 ml) and brine (100 ml), dried (MgSO4), filtered and concentrated under reduced pressure. The crude ester was dissolved in THF and aqueous 1 N NaOH solution was added. The solution was stirred at room temperature for 30 min. The THF was evaporated under reduced pressure and the residue was dissolved in aqueous 1 N NaOH solution. The solution was slowly acidified to pH 2 at 0° C. with aqueous 1 N HCl solution. The suspension was filtered and the resulting solid was rinsed with water and dried under reduced pressure to give the title compound (2.48 g, 92% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642277B2
Source datasetuspto-grants-2010_01
ORD IDord-35c8c0f67b7241feb41bc2376819755a
Source noteuspto-grants-2010_01