Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372667Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 178442784, compound

https://huagongshe.com/reaction/2372667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant(S)-2-fluorocaproic acidHCID 13683897—
Reactant(p-(5-Decyl-2-pyrimidinyl)phenoxymethyl]cyclohexanolHCID 86745590—
SolventDichloromethaneHCID 6344—
ProductHCID 178442784HCID 178442784—

Reaction Steps

0.62 g of trans-4-[(p-(5-decyl-2-pyrimidinyl)phenoxymethyl]cyclohexanol, 0.196 g of (S)-2-fluorocaproic acid, 0.413 g of dicyclohexylcarbodiimide and 0.025 g of 4-(dimethylamino)pydidine were dissolved in 25 ml of methylene chloride and stirred at room temperature for 15 hours. The white suspension was subsequently filtered. The residue obtained after evaporation of the solvent from the filtrate was purified by chromatography on silica gel with ethyl acetate/petroleum ether (vol. 1:9). Subsequent crystallization from 10 ml of ethyl acetate and 50 ml of hexane gave 0.62 g of trans-4-[(p-(5-decyl-2-pyrimidinyl)phenoxy)methyl]cyclohexyl (S)-2-fluorohexanoate as colourless crystals, m.p. (C-S) 88.5° C., phase transitions (S-SC) 108.8° C., (SC -SA) 128° C., cl.p. (SA -I) 137.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100577
Source datasetuspto-grants-1992_03
ORD IDord-e1b5f1f87795446398a45bfddc4d5934
Source noteuspto-grants-1992_03