HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29367Generated: October 26, 2026
1,2-Dimethoxyethane → 3-Methyl-4-pyridin-4-yl-benzofuran-2-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/29367
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (Pyridin-4-yl)boronic acid | HCID 2734379 | — |
| Reactant | 3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl ester | HCID 86599030 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Methyl-4-pyridin-4-yl-benzofuran-2-carboxylic acid tert-butyl ester | HCID 68716363 | 74.2% |
Reaction Steps
3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl ester (258 mg, 0.68 mmol) was mixed with K2CO3 (207 mg, 2.2 eq), pyridine-4-boronic acid (110 mg, 1.3 eq), Pd(Ph3)4 (43 mg, 0.05 eq), 3 mL of 1,2-dimethoxyethane and 0.5 mL of water. The mixture was heated and stirred in an 85° C. oil bath for 5 h. The reaction mixture was poured into water and was extracted with ethyl acetate. The organic extract was washed with water and dried over sodium sulfate. Removal of solvent gave the crude product, which was purified by column chromatography to give 156 mg of 3-methyl-4-pyridin-4-yl-benzofuran-2-carboxylic acid tert-butyl ester, obtained as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07420001B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-b31709faa8774b43adaf6d01d013a3d2 |
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| Source note | uspto-grants-2008_09 |
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