HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577394Generated: October 28, 2026
4-Aminothiophenol → HCID 58542087, compound
https://huagongshe.com/reaction/577394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminothiophenol | HCID 14510 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58542087 | HCID 58542087 | 75.7% |
Reaction Steps
To a suspension of sodium hydride (60% dispensed in mineral oil, 0.97 g, 24 mmol) in anhydrous tetrahydrofuran (80 mL), was added 4-aminobenzenethiol (2.77 g, 22 mmol) dissolved in tetrahydrofuran (20 mL) over 5 minutes. The mixture was stirred at room temperature for 30 minutes, to this was added a solution of 2,4-dichloropyrimidine (3.00 g, 20 mmol) dissolved in tetrahydrofuran (20 mL) over 5 minutes. The resulting mixture was stirred at room temperature for 64 hours, diluted with ethyl acetate (100 mL), washed with water and brine. After being dried (Na2SO4), the organic solution was concentrated in vacuo. The residue was flash chromatographed on silica gel using 5% of acetone in dichloromethane as eluant to give the product (3.60 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040549B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-19bcacfefbfa4303a110fd91c16d556a |
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| Source note | uspto-grants-2015_05 |
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