Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226077Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 178444060, compound

https://huagongshe.com/reaction/2226077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2,3-Difluoro-4-heptyloxybenzoic acidHCID 18965931—
ReactantHCID 178444450HCID 178444450—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 178444060HCID 17844406054.3%

Reaction Steps

1.9 g of 2,3-difluoro-4-heptyloxybenzoic acid, 2 g of 4-[4-(trans-4-pentylcyclohexyl)-1-butyl]phenol and 0.1 g of 4-(dimethylamino)pyridine were dissolved in 250 ml of dichloromethane and the solution was treated portionwise within 10 minutes while stirring with 1.6 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 sulfate, filtered and then concentrated. Chromatography of the residue on silica gel with toluene/ethyl acetate (vol. 4:1) and recrystallization from ethanol gave 2 g of 2,3-difluoro-4-heptyloxybenzoic acid 4-[4-(trans-4-pentylcyclohexyl)-1-butyl]phenyl ester with m.p. (C-SC) 67° C., SC -N 70° C. and cl.p. (N-I) 128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05346647
Source datasetuspto-grants-1994_09
ORD IDord-848f5003d9e94bc7a660667df16d53ed
Source noteuspto-grants-1994_09