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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432938Generated: November 2, 2026

Allyl bromide → 1-(2-Propenyl)-4-tert-butyloxycarbonyl-2-piperazinone

https://huagongshe.com/reaction/1432938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Propenyl)-4-tert-butyloxycarbonyl-2-piperazinoneHCID 5445238476%

Reaction Steps

4-(tert-Butyloxycarbonyl)-piperazin-2-one (1.0 g, 5.0 mmol), EXAMPLE 40, is alkylated with allyl bromide (0.48 ml, 5.5 mmol) in THF (20 ml) using the procedure described in Example 92, Part A. The title compound (0.92 g, 3.8 mmol) is obtained as a colorless liquid after chromatographed (50% ethyl acetate/hexane). EI MS m/z 240 (M+); 1H NMR (CDCl3, 300 MHz) δ5.80-5.68 (m, 1H), 5.23-5.15 (m, 2H), 4.09 (s, 2H), 4.03 (d, 2H), 3.63 (t, 2H), 3,30 (t, 2H), 1.45 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-281777f1be8248fd9c08489322caa3c7
Source noteuspto-grants-2009_11