Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648317Generated: October 28, 2026

Malic Acid → O-[4-(16-bromohexadecylamino)benzoyl]malic acid

https://huagongshe.com/reaction/648317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalic AcidHCID 525—
ReactantTriethylamineHCID 8471—
ReactantN-Carbobenzyloxy-4-(16-bromohexadecylamino)benzoyl chlorideHCID 20482544—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductO-[4-(16-bromohexadecylamino)benzoyl]malic acidHCID 86737437—

Reaction Steps

To a warm solution of N-carbobenzyloxy-4-(16-bromohexadecylamino)benzoyl 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, the solution is evaporated, and the residue is crystallized from acetic acid to yield the title compound as a tan, crystalline mass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04411903
Source datasetuspto-grants-1983_10
ORD IDord-09b95193f2cc4782849fe3f01ec2aa30
Source noteuspto-grants-1983_10