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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055948Generated: November 1, 2026

Isobutyl iodide → Rac-tert-butyl 5-isobutyl-2,4-dioxopiperidine-1-carboxylate

https://huagongshe.com/reaction/1055948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl iodideHCID 10556—
ReactantPotassium bisulfateHCID 516920—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactanttert-Butyl 2,4-dioxopiperidine-1-carboxylateHCID 23730999—
SolventTetrahydrofuranHCID 8028—
ProductRac-tert-butyl 5-isobutyl-2,4-dioxopiperidine-1-carboxylateHCID 6918394429.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of tert-butyl 2,4-dioxopiperidine-1-carboxylate (Ark Pharm, Inc., Libertyville, Ill.; 2.0 g, 9.389 mmol) in THF (1 L) at 20° C. was added LHMDS (1.0M in THF; 23.47 mL, 23.47 mmol) (dropwise), and the resulting mixture was stirred at 20° C. for 30 min. Isobutyl iodide (6.9 g, 37.55 mmol) was added, and the resulting mixture was stirred at 20° C. for 1 h. The mixture was neutralized with 10M aq. KHSO4 solution and extracted with EtOAc. The organic extract was dried over Na2SO4, filtered, and concentrated in vacuo to provide crude rac-tert-butyl 5-isobutyl-2,4-dioxopiperidine-1-carboxylate (0.75 g) (used without further purification in subsequent transformations): m/z (ESI, +ve) 170.0 [(M+H)-100]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394297B2
Source datasetuspto-grants-2016_07
ORD IDord-629d720fe507460da346ecbd62bd614c
Source noteuspto-grants-2016_07