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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625144Generated: October 30, 2026

2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → HCID 86718854, compound

https://huagongshe.com/reaction/625144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
Reactant4-Aminobenzyl alcoholHCID 69331—
ReactantHCID 68281804HCID 68281804—
SolventDichloromethaneHCID 6344—
ProductHCID 86718854HCID 8671885441.3%

Reaction Steps

In a pear-shaped flask, the above synthesized (S)-2-[(S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenyl-propionylamino]-hexanoic acid (10.72 g, 21 mmol, Eq: 1.00), (4-aminophenyl)methanol (2.717 g, 22 mmol, Eq: 1.03), and 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ) (7.994 g, 32 mmol, Eq: 1.50) were dissolved in CH2Cl2 (320 ml) and stirred overnight under a balloon of Ar. The mixture was poured onto crashed ice/NH4Cl, extracted 2× with AcOEt, washed with H2O, dried over Na2SO4, and the volume reduced to ˜300 ml. The precipitate was filtered off and dryed to give 5.25 g of the title compound as light-brown solid. MS (ISP): (M+H) 606.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301990B2
Source datasetuspto-grants-2016_04
ORD IDord-bbafeb9855984e1799e8d6fe06239535
Source noteuspto-grants-2016_04