HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911450Generated: November 1, 2026
4-Methylbenzenethiol → HCID 57656218, compound
https://huagongshe.com/reaction/911450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylbenzenethiol | HCID 7811 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86661654 | HCID 86661654 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57656218 | HCID 57656218 | 66.2% |
Reaction Steps
In a sealed tube dissolve 4-methylbenzenethiol (4.13 g, 33.2 mmol) in DMF (20 mL) at ambient temperature. Add portionwise with stirring sodium hydride (899 mg, 37.5 mmol) followed by tetrabutylammonium iodide (82 mg, 0.22 mmol) and a solution of methanesulfonic acid 3,3,3-trifluoro-2-methyl-2-trifluoromethylpropyl ester (6.16 g, 22.5 mmol) in DMF (10 mL). Stir at 150° C. overnight, cool the mixture to ambient temperature and dilute cautiously with water. Extract three times with EtOAc, dry over anhydrous Na2SO4, and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane to give the desired intermediate as a yellow oil (4.5 g, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022062B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-908321f374164cec9919083246ae1c8f |
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| Source note | uspto-grants-2011_09 |
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