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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726879Generated: October 31, 2026

HCID 19352281, compound → HCID 10868373, compound

https://huagongshe.com/reaction/726879

Reaction equation

Participants

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

Reaction Steps

2nd step--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 numberUS05710336
Source datasetuspto-grants-1998_01
ORD IDord-7eb53c0d1778410cae4c0a9615806cf6
Source noteuspto-grants-1998_01