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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881772Generated: November 1, 2026

HCID 86612635, compound → HCID 86612634, compound

https://huagongshe.com/reaction/1881772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86612635HCID 86612635—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
CatalystFerric cationHCID 29936—
SolventEthanolHCID 702—
ProductHCID 86612634HCID 8661263457%

Reaction Steps

17 (350 mg, 0.8 mmol) was suspended in 175 mL of EtOH. 10% (w/w, 38 mg) of 10% Pd/C catalyst was added to the hydrogenation flask (500 mL Pyrex® Parr reaction bottle tested to 120 psi, max. working pressure of 60 psi). The Parr hydrogenation system located in the VanNieuwenhze lab was used for the deprotection reactions. The hydrogen pressure was set to 35 psi with agitation, and the process went on for 41 h. A white precipitate was present even after the reaction was stopped, but this white product reacted with iron(III) to give a reddish product instead of no reaction as seen with the protected starting material. The catalyst was removed by vacuum filtration and separated from the product by dissolving the white precipitate in 125 mL hot CH2Cl2 and MeOH and THF. The clear solution was concentrated by rotary evaporation to yield a white solid. The solid was washed with MeOH to remove residual DCU to yield a white, feathery microcrystalline solid. Yield: 57%. 1H NMR (d6-DMSO, 400 MHz, 25° C.): δ 4.75 (s, 2H, —CH2—), 6.11 (t, J=7.0 Hz, 1H, Ar—H), 6.72 (d, J=7.2 Hz, 1H, Ar—H), 6.97 (m, 4H, Phenoxy-H), 7.11 (m, 2H, Ar—H, Phenoxy-H), 7.36 (t, J=7.2 Hz, 2H, Phenoxy-H), 7.58 (d, J=6.8 Hz, 2H, Phenoxy-H), 9.03 (s, 1H, —OH), 10.36 (s, 1H, APCI-MS: m/z 336.9 [M+H]+. Anal. Calcd for C19H16N2O4: C, 67.85; H, 4.79; N, 8.33. Found: C, 67.75; H, 5.07; N, 8.49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318945B2
Source datasetuspto-grants-2012_11
ORD IDord-1c266f646b05443e9b56aaeb9cebf067
Source noteuspto-grants-2012_11