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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278315Generated: November 3, 2026

Malic Acid → HCID 86737896, compound

https://huagongshe.com/reaction/1278315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalic AcidHCID 525—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 86737897HCID 86737897—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDiethyl EtherHCID 3283—
ProductHCID 86737896HCID 86737896—

Reaction Steps

A warm solution of 4-[N-carbobenzyloxy-(allylamino]phenylacetyl chloride and 1.3 g. triethylamine in 100 ml. ether is treated with 2 g. malic acid. An immediate precipitate forms, but the mixture is refluxed for one hour and filtered while hot. The solid is washed several times with hot ether, then the ether is evaporated to yield a white solid. The product is dissolved in tetrahydrofuran (100 ml.) and hydrogenated over 600 mg. 10% palladium-on-carbon at 50 psi until hydrogen uptake stops. The catalyst is filtered, and the solution is evaporated. The residue is crystallized from acetic acid to yield O-[4-(allylamino)phenylacetyl]malic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04281019
Source datasetuspto-grants-1981_07
ORD IDord-46618e4175354b70b7ae6a4803003f35
Source noteuspto-grants-1981_07