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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744881Generated: November 3, 2026

Trifluoroacetic acid → HCID 69943705, compound

https://huagongshe.com/reaction/744881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantHCID 69943109HCID 69943109—
ProductHCID 69943705HCID 6994370599.8%

Reaction Steps

A 1.32 g of 1-(p-methoxybenzyloxycarbonyl)-4-((2S)-4-(p-nitrobenzyloxycarbonyl) amino-2-hydroxybutyryl)piperazine was added to a mixture of 15 ml of trifluoroacetic acid and 1.35 ml of anisole, followed by 1 hour of reaction at room temperature. After removing trifluoroacetic acid by evaporation under a reduced pressure, a residue was adjusted to basic with sodium hydroxide and extracted with chloroform, and the organic layer was washed with water and dried over sodium sulfate, followed by evaporation of the solvent under a reduced pressure. Thereafter, the resulting residue was subjected to a silica gel column chromatography to yield 0.91 g of 1-((2S)-4-(p-nitrobenzyloxycarbonyl)amino-2-hydroxybutyryl)piperazine as a syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559224
Source datasetuspto-grants-1996_09
ORD IDord-018824ab7c844e9db8785c5138c5f1f5
Source noteuspto-grants-1996_09