Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 10827117 | HCID 10827117 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20195523 | HCID 20195523 | — |
Reaction Steps
The product of Step B is reacted in a Grignard reaction with 5 g. of magnesium turnings in 25 ml. of tetrahydrofuran (by adding the product of Step B in 150 ml. of tetrahydrofuran at a rate sufficient to sustain refluxing). Refluxing is continued for an additional 3 hours, after which the mixture is stirred overnight at about 20° C. To this reaction mixture is added gaseous carbon dioxide over a period of 1 hour, the mixture being maintained at reflux during the second half of the hour. The reaction mixture is cooled and cautiously added to 50 ml. of 6N hydrochloric acid, then evaporated to provide a residue which is recrystallized from acetic acid to provide tan crystals of 4-(5-methyl-3-benzofuranyl)benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04675320 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-6185f01800314585a96993c8d881e457 |
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| Source note | uspto-grants-1987_06 |
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