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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569626Generated: October 30, 2026

Diisopropylamine → 2,4-Bis(m-methoxyphenyl)butyric acid

https://huagongshe.com/reaction/569626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant(3-Methoxyphenyl)acetic acidHCID 15719—
ReactantLithium diisopropylamideHCID 2724682—
Reactant3-Methoxyphenethyl mesylateHCID 13061542—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2,4-Bis(m-methoxyphenyl)butyric acidHCID 12972204—

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of m-methoxyphenylacetic acid (1.33 g.) in tetrahydrofuran (10 ml.) was added to a stirred solution of lithium diisopropylamide, generated from diisopropylamine (2.1 ml.) and n-butyllithium (9.23 ml. of a 1.6 molar solution in hexane) in tetrahydrofuran (15 ml.), which was cooled to -70° C.; and the mixture was allowed to warm up to laboratory temperature, stirred at that temperature for 30 minutes and cooled to -70° C. A solution of 2-m-methoxyphenylethyl methanesulphonate (1.9 g.) in tetrahydrofuran (5 ml.) was added, the mixture was allowed to warm up to laboratory temperature and was stirred at that temperature for 18 hours, and water (50 ml.) was added. The mixture was washed with diethyl ether, acidified with aqueous 6N-hydrochloric acid and extracted three times with ethyl acetate (50 ml. each time). The combined extracts were washed with water, dried and evaporated to dryness and there was thus obtained as residue 2,4-bis-(m-methoxyphenyl)butyric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04732912
Source datasetuspto-grants-1988_03
ORD IDord-a6d63fbf90374c5ea8235a2f70c9c699
Source noteuspto-grants-1988_03