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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639Generated: October 23, 2026

Dicyclohexylcarbodiimide → HCID 178418275, compound

https://huagongshe.com/en/reaction/1639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant(E)-4-(trimethylsilyl)but-2-en-1-olHCID 21846715—
ReactantHCID 178418479HCID 178418479—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 178418275HCID 17841827538%

Reaction Steps

1.3 g of 4-trimethylsilyl-(E)-but-2-en-1-ol (synthesis described in J. Org. Chem. 1984, 49, 4092), 1.08 g of 6-hydroxy-nicotinic acid and 178 mg of 4-dimethylaminopyridine were placed in succession in 30 ml of abs. dimethylformamide. 1.77 g (1.1 eq.) of dicyclohexylcarbodiimide were added thereto at 0° and the mixture was left to react at room temperature overnight. The separated urea was filtered off, the filtrate was extracted with ethyl acetate, washed twice with H2O, dried over Na2 SO4 and the solvent was removed under reduced pressure. Flash chromatography on SiO2 (hexane/ethyl acetate=1/1) yielded 782 mg of 4-trimethylsilanyl-(E)-but-2-enyl 6-hydroxy-nicotinate as white crystals of m.p. 107°-110° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726191
Source datasetuspto-grants-1998_03
ORD IDord-998b94bdae2a4efb8c11261a196e92e3
Source noteuspto-grants-1998_03