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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393506Generated: November 2, 2026

HCID 20823149, compound → HCID 20823157, compound

https://huagongshe.com/reaction/1393506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20823149HCID 20823149—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 20823157HCID 20823157—

Reaction Steps

A solution of 3-(4-Benzyloxy-phenyl)-2-methyl-2-(quinolin-6-yloxy)-propionic acid ethyl ester (2.65 g, 6.0 mmol) in 100 mL of EtOH with 5% Pd/C (530 mg, 20 w %) was allowed to stand under 1 atm H2 for 6 h. Catalyst was filtered off and organic solvent was removed under vacuum. Residue was then dissolved in 200 mL of toluene. 530 mg of 10% Pd/C was added. The mixture was heated to reflux under air for overnight. Reaction was cooled to r.t. and catalyst was filtered off. Organic solvent was removed under vacuum and crude material was clean for next step without further purification. 1H NMR (400 MHz, CDCl3) δδ8.77 (dd, 1H, J=4.0, 1.4 Hz), 8.04 (d, 1H, J=7.6 Hz), 8.02 (d, 1H, J=9.6 Hz), 7.38 (dd, 1H, J=8.4, 4.4 Hz), 7.32 (dd, 1H, J=9.2, 2.8 Hz), 7.09 (d, 2H, J=8.8 Hz), 7.03 (d, 1H, J=2.8 Hz), 6.83 (d, 2H, J=8.8 Hz), 4.22 (q, 2H, J=7.1 Hz), 3.35, 3.13 (ABq, 2H, J=13.6 Hz), 1.52 (s, 3H), 1.19 (t, 3H, J=7.1 Hz). MS (ES+) m/z mass calcd for C21H22NO4 (m+1) 352, found 352.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345070B2
Source datasetuspto-grants-2008_03
ORD IDord-a423576a63db4d7cae6d2e1a9d99cf99
Source noteuspto-grants-2008_03