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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404635Generated: October 27, 2026

Dicyclohexylcarbodiimide → HCID 86688894, compound

https://huagongshe.com/reaction/404635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Quinuclidinol, (-)-HCID 91404—
Reactant(Morpholin-4-yl)(phenyl)acetic acid--hydrogen chloride (1/1)HCID 71432425—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86688894HCID 8668889423.5%

Reaction Steps

PS-DCC (loading: 1.25 mmol/g; 0.93 g, 1.16 mmol) was suspended in dry THF (11.6 ml) and HOBT (0.18 g, 1.16 mmol), 2-morpholino-2-phenylacetic acid hydrochloride (0.15 g, 0.58 mmol) and (R)-quinuclidin-3-ol (0.22 g, 1.75 mmol) were sequentially added. The mixture was shaken overnight and then PS-DCC was filtered off washing with EtOAc and THF. The solution was evaporated and the residue was dissolved in EtOAc (30 ml) and washed with water and then with a sat. NaHCO3. The organic phase was dried (Na2SO4), filtered and evaporated. The crude was purified by flash chromatography (DCM/MeOH=95/5 to 85/15) to obtain (R)-quinuclidin-3-yl 2-morpholino-2-phenylacetate (45 mg, 23.4% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748613B2
Source datasetuspto-grants-2014_06
ORD IDord-5885a27c348d47319f5a4eb3e37036c2
Source noteuspto-grants-2014_06