Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79498Generated: October 25, 2026

Diisopropylamine → 4-Tert-butyl 1-methyl 2-(4-chlorobenzyl)succinate

https://huagongshe.com/reaction/79498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantMethyl 3-(4-chlorophenyl)propanoateHCID 8027172—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Tert-butyl 1-methyl 2-(4-chlorobenzyl)succinateHCID 6873369681.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

BuLi (5.2 mL, 1.6M in hexanes) was added to a 0° C. solution of diisopropylamine (0.91 g, 9.0 mmol) in THF (40 mL). The reaction mixture was then stirred at 0° C. for 30 minutes, and then cooled to −78° C. A solution of methyl 3-(4-chlorophenyl)propanoate (1.5 g, 7.5 mmol) in THF (8 mL) was added slowly, and the reaction mixture was stirred at −78° C. for 40 minutes. A solution tert-butyl 2-bromoacetate (4.4 g, 22.7 mmol) in THF (5 mL) was then added. The reaction was then stirred for 30 minutes at −78° C. and then warmed to room temperature and stirred overnight. The reaction was then quenched with saturated NH4Cl and concentrated to remove THF. The reaction was then extracted with EtOAc, and the combined extracts were dried (Na2SO4), filtered, concentrated, and dried in vacuo to give 4-tert-butyl 1-methyl 2-(4-chlorobenzyl)succinate (1.91 g, 81%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841304B2
Source datasetuspto-grants-2014_09
ORD IDord-6674fe9f14df488cbb58d62056c61ab6
Source noteuspto-grants-2014_09