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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499265Generated: October 31, 2026

Methyl iodide → 4-Bromo-2-ethylbenzoic acid

https://huagongshe.com/reaction/1499265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant4-Bromo-2-methylbenzoic acidHCID 99570—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-2-ethylbenzoic acidHCID 10657005—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of LDA (10.7 mL, 21.39 mmol) in THF (20 mL) was added 4-bromo-2-methylbenzoic acid (2 g, 9.3 mmol) in THF (5 mL). The mixture was stirred at 0° C. for 1 h, cooled to −70° C., and then MeI (2.3 mL, 37.20 mmol) was added dropwise. The mixture was allowed to warm up to 0° C., stirred for 3 h, then quenched with H2O, and the pH was adjusted to 1-2 with 3 N HCl. The mixture was then diluted with water and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. Purification by normal phase silica gel column provided 4-bromo-2-ethylbenzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199994B2
Source datasetuspto-grants-2015_12
ORD IDord-affe056a671e43c48e64034e4d26e834
Source noteuspto-grants-2015_12