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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236489Generated: October 30, 2026

Diisopropylamine → 4-Tert-butyl-2-(carboxymethyl)benzoic acid

https://huagongshe.com/reaction/2236489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantDimethyl CarbonateHCID 12021—
Reactant4-Tert-butyl-2-methylbenzoic acidHCID 11958977—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Tert-butyl-2-(carboxymethyl)benzoic acidHCID 42625830—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a magnetically stirred solution of diisopropyl amine (0.75 g, 7.4 mmol) in THF (5 mL) at −30° C. is added BuLi (3.4 mL, 2.5 M in hexanes, 8.5 mmol). The mixture is stirred for 10 minutes at this temperature and cooled to −78° C. A solution of 4-tert-Butyl-2-methyl-benzoic acid [J. Am. Chem. Soc. 1944, 66, 154] (250 mg, 1.3 mmol) and dimethylcarbonate (150 mg, 1.67 mmol) in THF (3 mL) is added dropwise at −78° C. The mixture is allowed to stir at this temperature for 2 hours before it is allowed to warm to room temperature. The mixture is quenched with MeOH and water once it reached room temperature. After removal of THF, the water layer is extracted with ether. The water layer is acidified with HCl and the product is extracted from ether. After chromatography, the title compound is isolated pure (125 mg, 41%). MS (ESI): 237.1 (M+1)+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-f601c3286c17427caa1a2505a2a7ef38
Source noteuspto-grants-2010_05