HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092977Generated: October 31, 2026
Potassium Carbonate → 3-Benzyl-3-methyl-2,3-dihydro-benzofuran-6-carboxylic acid methyl ester
https://huagongshe.com/reaction/2092977
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 4-Iodo-3-(2-methyl-allyloxy)-benzoic acid methyl ester | HCID 25129045 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Benzyl-3-methyl-2,3-dihydro-benzofuran-6-carboxylic acid methyl ester | HCID 25129046 | 95.1% |
Reaction Steps
To a solution of 4-Iodo-3-(2-methyl-allyloxy)-benzoic acid methyl ester (455 mg, 1.37 mmol) obtained in Example 4(A), in DMF (15 mL) were added Potassium carbonate (379 mg, 2.74 mmol), Tetrabutylammonium chloride (380 mg, 1.37 mmol), Palladium acetate (25.6 mg, 0.136 mmol) in DMF (5 mL) and Phenylboronic acid (200 mg, 1.64 mmol). The resulting mixture was stirred for 3 h at 115° C., cooled to room temperature, filtered over silica, washed with water, dried over MgSO4 and concentrated. Column chromatography (silica gel, heptane/CH2Cl2: 4/6) afforded 368 mg (95%) of the title compound as a slightly brown oil which crystallize. Mp:52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440832B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-168d03f66ff44bb89bb469caab8f44a5 |
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| Source note | uspto-grants-2013_05 |
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