HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359635Generated: October 28, 2026
2-Methyl-2-butene → 5-(4-Chlorophenylthio)thiophene-2-carboxylic acid
https://huagongshe.com/reaction/1359635
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
The product of Step 33a (6. Ig, 24 mmol) is dissolved in a mixture of THF, t-BuOH, 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 room temperature 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 1N NaOH and washed two times with ether. The aqueous solution is then acidified to pH<6 with concentrated HCl and a precipitate formed. The precipitate is collected by filtration and washed with 0.5M KHSO4 then water. The solid is dried in vacuo to give the product (5.7 g, 87%). MS for C11H7ClO2S2 (ESI) (M−H)− m/z 269.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599916B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-fe6c173f6baf47e693ae2ddf0fdb0c4e |
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| Source note | uspto-grants-2003_07 |
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