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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165227Generated: November 1, 2026

Benzyl O-(O-benzyl-N-benzyloxycarbonyl-L-serinyl)-N-trifluoroacetyl-L-serinate → O-(L-serinyl)-N-trifluoroacetyl-L-serine

https://huagongshe.com/reaction/2165227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl O-(O-benzyl-N-benzyloxycarbonyl-L-serinyl)-N-trifluoroacetyl-L-serinateHCID 18639970—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductO-(L-serinyl)-N-trifluoroacetyl-L-serineHCID 18640004—

Reaction Steps

A mixture of benzyl O-(O-benzyl-N-benzyloxycarbonyl-L-serinyl)-N-trifluoroacetyl-L-serinate (1 g) and 10% palladium on activated carbon (1 g) in acetic acid (30 ml) was hydrogenated under hydrogen at 40 psi at room temperature for 6 hours. The reaction mixture was filtered with Celite (filter aid, trade mark, made by Nakarai Chemicals) and the filtrate was concentrated in vacuo and the residue was diluted with water (50 ml) and lyophylized to give O-(L-serinyl)-N-trifluoroacetyl-L-serine (430 ml).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939241
Source datasetuspto-grants-1990_07
ORD IDord-d644a460fa7b466aabd2d7754067c494
Source noteuspto-grants-1990_07