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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165485Generated: October 31, 2026

Diisopropylamine → 2-dodecylbenzoic Acid

https://huagongshe.com/reaction/2165485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant2-Methylbenzoic acidHCID 8373—
Reactant1-BromoundecaneHCID 12744—
ReactantLithium diisopropylamideHCID 2724682—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-dodecylbenzoic AcidHCID 122418—

Reaction Steps

A solution containing lithium diisopropylamide (0.1 mole) was prepared by treating a solution of diisopropylamine (14.1 ml, 0.1 mole) in tetrahydrofuran (200 ml) at 0° C. with n-butyl lithium (41.2 ml of a 2.43 M solution, 0.1 mole), and stirring for 5 minutes. To this was added a solution of o-toluic acid (6.8 g, 0.05 mole) in tetrahydrofuran (50 ml). The ice bath was removed and the intense red solution was stirred for 30 minutes. This solution was slowly pipetted into a solution of undecylbromide (11.8 g, 0.05 mole) in tetrahydrofuran (50 ml) at -20° C. After the addition, the cooling bath was removed and the solution stirred for 30 minutes. A small amount of water was added and most of the tetrahydrofuran was removed under reduced pressure The residue was poured into water, acidified with 3N hydrochloric acid and extracted with ether. The ether was dried, evaporated and the residue was recrystallized from acetonitrile, then from hexane, to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939279
Source datasetuspto-grants-1990_07
ORD IDord-1232ae4bb6a84e5ebcb51e33d0ff7ac2
Source noteuspto-grants-1990_07