HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274106Generated: October 30, 2026
Hydrochloric Acid → HCID 14316717, compound
https://huagongshe.com/reaction/274106
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | 3-Furoic acid | HCID 10268 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14316717 | HCID 14316717 | 15.1% |
Reaction Steps
70.7 g of p-toluidine, cooled with a bath of water and ice, are treated with 205 ml of 36% HCl. The mixture is then stirred at 55°-60° C. for 30 min before being cooled to 0° C. again. A solution of 45 g of NaNO2 in 220 ml of water is then introduced. The mixture is stirred for 1 h at 0° C. This cold solution is introduced into a mixture of 49.3 g of 3-furanoic acid, 220 ml of acetone, 23.4 g of CuCl2 and 6.3 g of water, cooled to -5° C. The whole is stirred at 0° C. for 2 h and then at room temperature for 48 h. It is extracted twice with ether and the organic phase is decanted, dried and concentrated to give an oil, which gives crystals when treated with water. The crystals are filtered off and washed with 50 ml of a 50% methanol/water mixture to give 13.4 g of 2-(4-methylphenyl)-3-furanoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387747 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-cba1164fe76c41acaf6b5528da40c795 |
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| Source note | uspto-grants-1995_02 |
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