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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108566Generated: October 30, 2026

Methyl iodide → Tert-butyl 4-methyl-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/1108566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-methyl-3-oxopiperazine-1-carboxylateHCID 1878391673.3%

Reaction Steps

1-tert-Butoxycarbonyl-3-oxopiperazine (see Tetrahedron Lett. (1980), 21(32), 3019-20 for outline of synthesis, 5 g) was dissolved in dry DMF (75 ml) and potassium tert-butoxide (3.08 g) was added. The mixture was stirred at ambient temperature for 1 hour, then iodomethane (3.9 g) was added, and stirring continued at the same temperature for 2.5 hours. Solvent was evaporated, and the residue chromatographed on silica, using as eluant a gradient increasing in polarity from 0 to 100% ethyl acetate in iso-hexane. Relevant fractions were combined and evaporated to give 1-tert-butoxycarbonyl-4-methyl-3-oxopiperazine (3.92 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069145
Source datasetuspto-grants-2000_05
ORD IDord-5d42a03af54f46bbab768f2f59cea513
Source noteuspto-grants-2000_05