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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461497Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 19980018, compound

https://huagongshe.com/reaction/1461497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-chloro-3-methylbutanoic acidHCID 313493—
ReactantHCID 19809977HCID 19809977—
ReactantPotassium tert-butoxideHCID 23665647—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 19980018HCID 19980018—

Reaction Steps

A mixture of 5.3 g of p-[p-(4-cyano-4-octylcyclohexyl)-phenyl]phenol (obtainable by alkaline ether splitting from r-1-cyano-cis-4-(4'-propyloxybiphenyl-4-yl)-1-octylcyclohexane with potassium tert-butylate in NMP at 180°), 1.9 g of optically active 2-chloro-3-methylbutyric acid and 170 g of DMAP are suspended in 40 ml of CH2Cl2. 3.1 g of DCC in 5 ml of CH2Cl2 are then added dropwise at 0° and stirring is carried out for 12 hours at room temperature. After separating off the dicyclohexylurea and the usual working up, optically active 4'-(4-cyano-4-octylcyclohexyl)-biphenyl-4-yl 2-chloro-3-methylbutyrate is obtained, K 81 SA 138 I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075032
Source datasetuspto-grants-1991_12
ORD IDord-9abc8a76351f4619a6c35170b0261553
Source noteuspto-grants-1991_12