Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244483Generated: November 2, 2026

Dicyclohexylcarbodiimide → HCID 86600355, compound

https://huagongshe.com/reaction/1244483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3-(3,5-Ditert-butyl-4-hydroxyphenyl)prop-2-enoic acidHCID 99819—
Reactant4-Amino-2-NitrophenolHCID 3417419—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86600355HCID 8660035573.9%

Reaction Steps

1.78 g (6.4 mmoles) of 3,5-di-tert-butyl-4-hydroxycinnamic acid, 0.99 g (6.4 mmoles) of 4-amino-2-nitrophenol, previously diluted in 10 ml of DMF, 0.86 g (6.4 mmoles) of hydroxybenzotriazol and 1.32 g (6.4 mmoles) of dicyclohexylcarbodiimide are introduced into a 50 ml flask containing 10 ml of THF. The reaction medium is agitated for 15 hours at ambient temperature, the precipitate which appears is filtered and rinsed with ethyl acetate. After concentration of the solution under reduced pressure, the residue is diluted in 20 ml of ethyl acetate and the insoluble part is filtered again. The filtrate is washed with 20 ml of a saturated solution of sodium carbonate followed by 20 ml of water and 20 ml of a saturated solution of sodium chloride. After drying over sodium sulphate, the organic solution is filtered and concentrated to dryness under reduced pressure. The residue is purified on a silica column (eluant: heptane/ethyl acetate: 8/2). The pure fractions are collected and concentrated under vacuum to produce 1.95 g (47%) of the expected compound in the form of a yellow-orange powder. Melting point: 231-232° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122535B2
Source datasetuspto-grants-2006_10
ORD IDord-fdb2fa1bb1364a6bb3937d9516848cd1
Source noteuspto-grants-2006_10