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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846496Generated: October 30, 2026

Sodium hydride → HCID 14349354, compound

https://huagongshe.com/reaction/846496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-IodopropaneHCID 33643—
ReactantHCID 136207173HCID 136207173—
Catalyst18-Crown-6HCID 28557—
SolventDimethylformamideHCID 6228—
ProductHCID 14349354HCID 1434935419.5%

Reaction Steps

To a stirred mixture of 0.24 g (0.005 mole) of sodium hydride (60% oil suspension) in 45 mL of N,N-dimethylformamide was added 1.3 g (0.005 mole) of 1,4-dihydro-1-(2,4,5-trichlorophenyl)-5H-tetrazol-5-one. The mixture was stirred at room temperature for 15 minutes, then 0.85 g (0.005 mole) of 1-iodopropane and several drops of 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6) were added. After complete addition, the reaction mixture was stirred at room temperature for 4 days. The reaction mixture was poured into ice water and the resulting mixture extracted with diethyl ether. The ether extract was dried over anhydrous magnesium sulfate, filtered, and the filtrate evaporated under reduced pressure to leave a solid. The solid was purified by column chromatography on silica gel, eluting with methylene chloride. Recrystallization from ethanol gave 0.3 g of 1,4-dihydro-4-propyl-1-(2,4,5-trichlorophenyl)-5H-tetrazol-5-one as a solid, mp 89°-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05136868
Source datasetuspto-grants-1992_08
ORD IDord-59c93a1c9e5b4cfba1a00708fd472454
Source noteuspto-grants-1992_08