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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267967Generated: October 30, 2026

Water → HCID 18348181, compound

https://huagongshe.com/reaction/2267967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoroethyl bromideHCID 12982—
Reactant5-(4-Methylphenyl)-1H-tetrazoleHCID 285164—
SolventAcetonitrileHCID 6342—
ProductHCID 18348181HCID 1834818143.8%

Reaction Steps

Under a nitrogen atmosphere, a stirred solution of 5.0 grams (0.031 mole) 4-(4-methylphenyl)-1,2,3,5-(1H)-tetrazole and 4.8 grams (0.035 mole) of potassium carbonate in 150 mL of acetonitrile was heated to reflux and then cooled to ambient temperature. To this was slowly added 10.0 grams (0.078 mole) of 1-bromo-2-fluoroethane. Upon completion of the addition the reaction mixture was placed in a water bath and cooled to 0° C., where it stirred for one hour. After this time the reaction mixture was heated to reflux, where it stirred for three hours, and then cooled to 0° C., where it stirred for about 18 hours. At the conclusion of this period the reaction mixture was poured into 50 mL of water. The resulting solution was extracted with three 50 mL portions of ethyl acetate. The combined extracts were concentrated under reduced pressure to a residue, which was subjected to column chromatography on silica gel. Elution was accomplished with methylene chloride and acetone. The product-containing fractions were combined and concentrated under reduced pressure, yielding 2.8 grams 1-(2-fluoroethyl)-(4-methylphenyl)-1,2,3,5-(1H)-tetrazole. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSH0002007H1
Source datasetuspto-grants-2001_12
ORD IDord-9ec13a3d4ad3458d996cabd1ea83c885
Source noteuspto-grants-2001_12