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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725835Generated: October 30, 2026

Acetic Anhydride → HCID 178474959, compound

https://huagongshe.com/reaction/725835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant3-(4-Aminophenyl)propionic acidHCID 75451—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventWaterHCID 962—
ProductHCID 178474959HCID 178474959—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 397 g of 3-(4-amino-phenyl)propionic acid, 125 g of NaOH and 160 g of Raney nickel in 5.71 of water is hydrogenated at 170° C. and 100 bar until no further hydrogen is taken up (30 hours). After filtration and washing the residue with water, 6.31 of a colourless solution are obtained as the filtrate, which is combined with a solution of 129 g of NaOH in 400 ml of water, after which 454 ml of acetic anhydride are added dropwise thereto within 35 minutes. After 5 hours the precipitate is filtered off, the filtrate is adjusted to pH 4 by the addition of concentrated hydrochloric acid and stirred for 3 hours at 0° C. It is then suction filtered, washed with 250 ml of ice water and dried at 70° C. In this way, 216 g of 3-(trans-4-acetylaminocyclohexyl)propionic acid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05707989
Source datasetuspto-grants-1998_01
ORD IDord-741f1f6dcd12400f872e8baab9a0a062
Source noteuspto-grants-1998_01