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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715701Generated: October 26, 2026

3,4,5-Trimethoxybenzonitrile → HCID 178487380, compound

https://huagongshe.com/reaction/715701

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxybenzonitrileHCID 15892—
Reactant2-Methylnicotinic acidHCID 643373—
ReactantLithium diisopropylamideHCID 2724682—
ReactantMethanedione--ethanol (1/1)HCID 19604758—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178487380HCID 178487380—

Reaction Conditions

Temperature0 °C

Reaction Steps

7 g 2-Methyl-nicotinic acid was suspended in 150 mL of tetrahydrofuran, and cooled to −70° C. with a bath of ethanol/dry ice. 80 mL lithium diisopropylamide (2.0 M in tetrahydrofuran/n-heptane/ethylbenzene) was added dropwise over 10 min and the mixture was stirred for 2 h at 0° C. Then it was cooled to −73° C. and a solution of 10 g 3,4,5-trimethoxy-benzonitrile (4.24) in 50 mL tetrahydrofuran was added. Then the reaction mixture was warmed overnight to ambient temperature. 30 mL Water was added and the solvent was distilled off before 200 mL ethyl acetate was added and the precipitate that formed was collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187478B2
Source datasetuspto-grants-2015_11
ORD IDord-6323fba206c947c0ab6d6554ac4e6c86
Source noteuspto-grants-2015_11