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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248931Generated: October 31, 2026

N-(5,7-dichloro-2,3-dihydrobenzofuran-2-ylmethyl)-N-butylcarbamyl chloride → 1-(N-(5,7-dichloro-2,3-dihydrobenzofuran-2-ylmethyl)-N-butylcarbamyl)-1,2,4-triazole

https://huagongshe.com/reaction/1248931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5,7-dichloro-2,3-dihydrobenzofuran-2-ylmethyl)-N-butylcarbamyl chlorideHCID 13563317—
Reactant1,2,4-TriazolylsodiumHCID 54719965—
SolventTetrahydrofuranHCID 8028—
Product1-(N-(5,7-dichloro-2,3-dihydrobenzofuran-2-ylmethyl)-N-butylcarbamyl)-1,2,4-triazoleHCID 1356331988.7%

Reaction Conditions

Temperature65 °C

Reaction Steps

13.5 g (0.04 mole) of N-(5,7-dichloro-2,3-dihydrobenzofuran-2-ylmethyl)-N-butylcarbamyl chloride were added dropwise to a suspension of 5.5 g (0.06 mole) of sodium 1,2,4-triazolide in 120 ml of dry tetrahydrofuran at 20° C. The mixture was stirred for 6 hours at 65° C., after which it was cooled to 20° C., and the precipitate was filtered off under suction. The filtrate was evaporated down, the residue was suspended in 30 ml of diethyl ether, and the product was filtered off under suction. 13.1 g of 1-(N-(5,7-dichloro-2,3-dihydrobenzofuran-2-ylmethyl)-N-butylcarbamyl)-1,2,4-triazole were obtained as colorless crystals of melting point 122°-124° C. (compound NO. 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04628058
Source datasetuspto-grants-1986_12
ORD IDord-93532d0c347b4f2fa44558b967e4ab14
Source noteuspto-grants-1986_12