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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981611Generated: November 3, 2026

1-Benzylpiperazin-2-one hydrochloride → Tert-butyl 4-benzyl-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/1981611

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzylpiperazin-2-one hydrochlorideHCID 12744519—
Reactant2-(t-Butoxycarbonyloxyimino)-2-phenylacetamideHCID 53719090—
SolventBenzeneHCID 241—
ProductTert-butyl 4-benzyl-3-oxopiperazine-1-carboxylateHCID 10891590—

Reaction Steps

A mixture of 1-(phenylmethyl)piperazinone (XIV, Example 40, 19.0 g., 0.1 mole) and 2-(t-butoxycarbonyloxyimino)-2-phenylacetamide (30.0 g., 0.12 mole) in benzene (200 ml.) is heated under reflux for 1 hour. The benzene is removed under reduced pressure, the residual oil is dissolved in ethyl acetate:SSB (1:1) and chromatographed on silica gel. The column is eluted with ethyl acetate, the appropriate fractions are pooled, concentrated and the product is crystallized from ethyl acetate:SSB (1:10) to give the title compound, m.p. 89°-90°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04593098
Source datasetuspto-grants-1986_06
ORD IDord-51a03b8ea53f42cbb1ec94969125f184
Source noteuspto-grants-1986_06