Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846511Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 19882813, compound

https://huagongshe.com/reaction/846511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-Butyn-1-olHCID 12991—
ReactantHCID 19882809HCID 19882809—
SolventAcetonitrileHCID 6342—
ProductHCID 19882813HCID 1988281320.7%

Reaction Steps

To a stirred solution of 0.5 g (0.0017 mole) of 1-(2,4-dichloro-5-hydroxyphenyl)-1,4-dihydro-4-propyl-5H-tetrazol-5-one (Example 10, Step A) and 0.15 g (0.0021 mole) of 2-butyn-1-ol in 5 mL of acetonitrile was added 0.33 g (0.0016 mole) of dicyclohexylcarbodiimide. The reaction mixture was heated at reflux temperature for 4 days, cooled to room temperature, and filtered. The filtrate was washed with 10 mL of a 10% aqueous sodium hydroxide solution, diluted with methylene chloride, and washed with 10 mL of 6N hydrochloric acid. The washed organic phase was dried over anhydrous magnesium sulfate, filtered, and the filtrate evaporated to leave an oil. The oil was purified by column chromatography on silica gel, eluting with ethyl acetate: heptane (20:80), to yield 0.12 g of 1-[2,4-dichloro-5-(2-butynyloxy)phenyl]-1,4-dihydro-4-propyl-5H-tetrazol-5-one as a solid, mp 58°-60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05136868
Source datasetuspto-grants-1992_08
ORD IDord-f1aec66fef634e2e88c8e4b96bd86973
Source noteuspto-grants-1992_08