Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636637Generated: October 29, 2026

HCID 19352281, compound → HCID 10868373, compound

https://huagongshe.com/reaction/1636637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19352281HCID 19352281—
CatalystPalladiumHCID 23938—
ProductHCID 10868373HCID 10868373—

Reaction Steps

The step consists in the catalytic hydrogenation of 3-benzyloxycarbonylamino-5-(2,3-dimethoxyphenyl)-2,5-dihydrofuran-2-one, for example with palladium on carbon as catalyst in alcoholic medium, thus obtaining directly in a single step the deprotected 2-amino-4-(2,3-dimethoxyphenyl)butyric acid. The reaction takes place in nearly quantitative yields. The reaction, as already discussed in the above process, can be carried out under enantioselectivity conditions, to obtain 2-amino-4-(2,3-dimethoxyphenyl)butyric acid in an optically active form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034277
Source datasetuspto-grants-2000_03
ORD IDord-bf4172861429425fb8a870b76e2a7a43
Source noteuspto-grants-2000_03