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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086776Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 178443276, compound

https://huagongshe.com/reaction/1086776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2,3-Difluoro-4-dodecyloxybenzoic acidHCID 15854522—
ReactantHCID 178444470HCID 178444470—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 178443276HCID 178443276—

Reaction Steps

2.0 g of 2,3-difluoro-4-dodecyloxybenzoic acid, 1.8 g of 4-[(E)-3-(trans-4-pentylcyclohexyl)allyloxy]phenol and 0.1 g of 4-(dimethylamino)pyridine were dissolved in 50 ml of dichloromethane and the solution was treated portionwise within 10 minutes while stirring with 1.4 g of N,N'-dicyclohexylcarbodiimide. The mixture was stirred at room temperature overnight and then filtered. The filtrate was diluted with dichloromethane, washed twice with 50 ml of saturated sodium carbonate solution each time and then with water, dried over magnesium sulphate and concentrated. The crude product obtained was purified by chromatography on silica gel with toluene. The 2,3-difluoro-4-dodecyloxybenzoic acid 4-[(E)-3-(trans-4-pentylcyclohexyl)allyloxy]phenyl ester obtained was recrystallized from ethanol; m.p. (C-SC) 73° C., SC -N 124° C., cl.p. (N-I) 137° C..

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05032312
Source datasetuspto-grants-1991_07
ORD IDord-f17b67e25c4f454e85a430802795f59f
Source noteuspto-grants-1991_07