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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265909Generated: October 30, 2026

(4-Nitrophenyl)acetic acid → HCID 178511529, compound

https://huagongshe.com/reaction/2265909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Nitrophenyl)acetic acidHCID 4661—
ReactantSodium HydroxideHCID 14798—
CatalystNickelHCID 935—
CatalystWaterHCID 962—
SolventWaterHCID 962—
ProductHCID 178511529HCID 178511529—

Reaction Conditions

Temperature125 °C

Reaction Steps

(4-Nitro-phenyl)-acetic acid (50 g, 276 mmol) was added to a stirred solution of 22.08 g of 50% sodium hydroxide solution in 450 mL deionizated water. The clear yellow solution is transferred into a high-pressure autoclave that it charged with 30 g (511 mmol) of water-wet sponge nickel catalyst. The autoclave is sealed, flushed with nitrogen and then pressurized to 115 bar with hydrogen. The reaction mixture is stirred and heated to 125° C. for 48 h. At that time the autoclave is cooled, vented and charged under nitrogen with another 30 g (511 mmol) of the sponge nickel catalyst. The autoclave is flushed again with nitrogen and then pressurized to 115 bar and the vessel is heated to 130° C. while stirring (a maximum pressure of 130 bars is observed). Hydrogenation is continued for 5 days to 130° C. The autoclave is then cooled, vented and flushed with nitrogen and the contents are removed and filtered through filter aid to remove catalyst. After removal of the solvent 74 g of crude material was obtained. The intermediated is used directly in the next step without purification. MS (m/e): 158.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858630B2
Source datasetuspto-grants-2010_12
ORD IDord-d8632c24424a4fa3b02dfde050cc6f01
Source noteuspto-grants-2010_12