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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4,5-Trimethoxybenzonitrile | HCID 15892 | — |
| Reactant | 2-Methylnicotinic acid | HCID 643373 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Methanedione--ethanol (1/1) | HCID 19604758 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178487380 | HCID 178487380 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187478B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-6323fba206c947c0ab6d6554ac4e6c86 |
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| Source note | uspto-grants-2015_11 |
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