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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209431Generated: October 26, 2026

Diisopropylamine → 3-Phenyl-2-t-butylcarboxymethylpropionic acid, ethyl ester

https://huagongshe.com/reaction/2209431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantEthyl 3-phenylpropionateHCID 16237—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-Phenyl-2-t-butylcarboxymethylpropionic acid, ethyl esterHCID 8674901246%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve diisopropylamine (3.5 mL, 25 mmol) in tetrahydrofuran (30 mL). Add n-butyllithium (14 mL of a 1.6M solution in hexane, 22.4 mmol). Stir for 15 minutes and cool to -78° C. Add, by dropwise addition, ethyl dihydrocinnamate (3.5 mL, 20 mmol) and stir for 30 minutes. Add t-butyl bromoacetate (4.0 mL, 25 mmol) and gradually warm to room temperature overnight. Quench the solution with ammonium chloride solution (10 mL) and partition between water (25 mL) and ethyl ether (50 mL). Separate the organic phase, dry (MgSO4) and evaporate the solvent in vacuo. Purify by silica gel chromatography (5% ethyl acetate/hexane) to give 3-phenyl -2-t-butylcarboxymethylpropionic acid, ethyl ester as a pale yellow oil (2.68 g, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455242
Source datasetuspto-grants-1995_10
ORD IDord-afc23055498143a996f97237774e972b
Source noteuspto-grants-1995_10