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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43354Generated: October 25, 2026

Methyl isobutyrate → 1,1-Dimethylethyl (2R,6S)-4-({4-[1,1-dimethyl-2-(methyloxy)-2-oxoethyl]phenyl}methyl)-2,6-dimethyl-1-piperazinecarboxylate

https://huagongshe.com/reaction/43354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl isobutyrateHCID 11039—
ReactantLithium dicyclohexylamideHCID 10932176—
Reactant1,1-Dimethylethyl (2R,6S)-4-[(4-bromophenyl)methyl]-2,6-dimethyl-1-piperazinecarboxylateHCID 25224097—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
Catalyst1,5-Diphenylpenta-1,4-dien-3-one;palladiumHCID 154270—
SolventTolueneHCID 1140—
Product1,1-Dimethylethyl (2R,6S)-4-({4-[1,1-dimethyl-2-(methyloxy)-2-oxoethyl]phenyl}methyl)-2,6-dimethyl-1-piperazinecarboxylateHCID 2522420665.5%

Reaction Steps

A solution of methyl 2-methylpropanoate (188 ul, 1.64 mmol) in toluene (3 ml) was added to lithium dicyclohexylamide (362 mg, 1.93 mmol) under glove bag conditions. The suspension was stirred for 10 mins then added to a mixture of D43 (570 mg, 1.49 mmol) and bis(dibenzylideneacetone) palladium (0) (43 mg, 0.074 mmol). Tri(tert-butyl)phosphine (18 ul, 0.074 mmol) was added and the reaction mixture stirred at room temperature overnight. The solvent was removed in vacuo and chromatography eluting with 0-90% EtOAc/petroleum ether gave the title compound as a yellow oil (395 mg). δH (CDCl3, 250 MHz) 7.29 (4H, m), 4.07 (2H, m), 3.66 (3H, s), 3.46 (2H, s), 2.61 (2H, m), 2.12 (2H, dd), 1.58 (6H, s), 1.46 (9H, s), 1.29 (6H, d). MS (ES): MH+ 405.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536182B2
Source datasetuspto-grants-2013_09
ORD IDord-c5561e98662a4bdd91f7af42e78611f5
Source noteuspto-grants-2013_09