HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412007Generated: October 26, 2026
2-Methyl-2-butene → 5-(4-Chlorophenylthio)thiophene-2-carboxylic acid
https://huagongshe.com/reaction/412007
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 5-[(4-Chlorophenyl)sulfanyl]-2-thiophenecarbaldehyde | HCID 7062194 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(4-Chlorophenylthio)thiophene-2-carboxylic acid | HCID 22350402 | 87.7% |
Reaction Steps
5-(4-Chlorophenylsulfanyl)thiophene-2-carboxaldehyde (6.1 g, 24 mmol) is dissolved in a mixture of THF, tBuOH, and water (3:3:1, 255 mL). 2-methyl-2-butene (20.3 mL, 192 mmol) is added followed by KH2PO4 (9.8 g, 72 mmol) and then NaClO2 (80%, 8.17 g, 72.3 mmol). The mixture is stirred at rt for 2 hours. Aqueous KHSO4 (0.5M, 200 mL) is added and the organic solvents are removed in vacuo to produce an aqueous suspension of the product. The precipitate is collected by filtration, dissolved in IN NaOH and washed two times with ether. The aqueous solution is then acidified to pH<2 with concentrated HCl and a precipitate formed. The precipitate is collected by filtration and washed with 0.5M NaHSO4 then water. The solid is dried in vacuo to give 5.7 g (87%) of 5-(4-chlorophenylsulfanyl)thiophene-2-carboxylic acid. MS for C11H7ClO2S2, (ES) m/z: 269 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562816B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-291cb619609d471896591303a306e1b1 |
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| Source note | uspto-grants-2003_05 |
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