HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251622Generated: October 31, 2026
Triethylborane → 6-(2,6-Diethyl-phenyl)-4-ethyl-2-methyl-nicotinic acid ethyl ester
https://huagongshe.com/reaction/251622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylborane | HCID 7357 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethyl 4-chloro-6-(2,6-diethylphenyl)-2-methylnicotinate | HCID 59678345 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-(2,6-Diethyl-phenyl)-4-ethyl-2-methyl-nicotinic acid ethyl ester | HCID 66993641 | 64.3% |
Reaction Steps
A mixture of 4-chloro-6-(2,6-diethyl-phenyl)-2-methyl-nicotinic acid ethyl ester (251 mg, 0.76 mmol), triethylborane (4.6 mL of 1 M solution in hexane, 4.6 mmol), Pd(PPh3)4 (26 mg, 0.023 mmol), and Na2CO3 (1.27 g, 6 mL of 2M solution in H2O) in toluene (20 mL) is heated for 48 hours at 95° C. After cooling to room temperature the mixture is diluted with water (10 mL) and extracted with EtOAc. The combined extracts are washed with saturated brine, dried (Na2SO4), concentrated, and purified by flash chromatography (elution with hexane/EtOAc 10:1) to yield 159 mg 6-(2,6-diethyl-phenyl)-4-ethyl-2-methyl-nicotinic acid ethyl ester as a colorless oil: 1H NMR (CDCl3) 7.29 (dd, 1H), 7.13 (d, 2H), 7.00 (s, 1H), 4.47 (q, 2H), 2.68 (q, 2H), 2.59 (s, 3H), 2.0-2.3.7 (m, 4H), 1.45 (t, 3H), 1.24 (t, 3H), 1.05 (t, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863454B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-841444e41b6e45f8bf17acfd30cf59c5 |
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| Source note | uspto-grants-2011_01 |
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