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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416416Generated: November 3, 2026

1-Butanol → HCID 178437930, compound

https://huagongshe.com/reaction/1416416

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantSulfuric AcidHCID 1118—
ReactantSodium AzideHCID 33557—
ReactantHCID 15859426HCID 15859426—
CatalystZincchlorideHCID 3007855—
SolventChloroformHCID 6212—
ProductHCID 178437930HCID 17843793079%

Reaction Conditions

Temperature115 °C

Reaction Steps

In a 500-ml glass-made reactor equipped with a thermometer and a reflux condenser, 200 ml of n-butanol, 37.5 g of zinc chloride and 50.7 g of sodium azide were charged, followed by stirring for 30 minutes. To the reactor, 50 g of 5-ethyl-2-imino-3-(2'-cyanobiphenyl-4-yl)methyl-1,3,4-thiadiazoline were charged further, followed by heating the internal temperature to 110 to 120° C. at which the reaction was effected for 20 hours. After the completion of the reaction, the reaction mixture was cooled. After the internal temperature decreased to 100° C. or lower, adequate amounts of chloroform and 10% sulfuric acid were added to the reaction mixture, followed by stirring for 30 to 60 minutes. The reaction mixture was cooled and then separated. To the organic layer, a 5% aqueous solution of sodium hydroxide was added. The resulting mixture was stirred for several hours, followed by separation into layers. The aqueous layer was adjusted to pH 7 with 3N hydrochloric acid. The white crystals so precipitated were collected by filtration. The crude crystals so obtained were washed with chloroform under heating and then cooled to room temperature. After cooling to room temperature, the reaction mixture was collected by filtration and dried, whereby about 44.8 g of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912353
Source datasetuspto-grants-1999_06
ORD IDord-0673c82a484d4dd48e9bd02618f70f60
Source noteuspto-grants-1999_06