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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325563Generated: October 30, 2026

Malic Acid → HCID 86739349, compound

https://huagongshe.com/reaction/325563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalic AcidHCID 525—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 86737897HCID 86737897—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDiethyl EtherHCID 3283—
ProductHCID 86739349HCID 86739349—

Reaction Steps

A warm solution of 3-[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-[3-(allylamino)phenylacetyl]malic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04440940
Source datasetuspto-grants-1984_04
ORD IDord-76510484163f43bb8bcc9a804a281b82
Source noteuspto-grants-1984_04