HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958683Generated: October 31, 2026
4-Methoxyphenylacetic Acid → HCID 67184281, compound
https://huagongshe.com/reaction/1958683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxyphenylacetic Acid | HCID 7690 | — |
| Reactant | Methyl 2-chlorobenzoate | HCID 11895 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 6930993 | HCID 6930993 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67184281 | HCID 67184281 | — |
Reaction Steps
5-(2-Chlorophenyl)-4-(4-methoxyphenyl)thiophene-2-carboxylic acid is prepared, according to the procedure used in stages 1A)-1E), from (4-methoxyphenyl)acetic acid and methyl 2-chlorobenzoate. In the final stage of this procedure, 5 g of methyl 542-chlorophenyl)-4-(4-methoxyphenyl)-2-thiophenecarboxylate and 1.11 g of sodium hydroxide pellets are added to 30 ml of methanol and 3 ml of dioxane. The reaction medium is heated at 50-60° C. for 5 hours. It is evaporated to dryness, water is added and the impurities are extracted with ether. The aqueous phase is acidified and the expected compound is extracted with ether. After drying and evaporating, 3.5 g of the expected compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410137B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-0181be645ad54182b57b81c5e8d0686a |
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| Source note | uspto-grants-2013_04 |
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