HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901390Generated: October 31, 2026
4-Toluenesulfonyl chloride → HCID 59699753, compound
https://huagongshe.com/reaction/901390
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Reactant | HCID 59699729 | HCID 59699729 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Bromide | HCID 253881 | — |
| Product | HCID 59699753 | HCID 59699753 | 55% |
Reaction Steps
2.82 g (9.75 mmol) of 4-(5-bromo-1H-pyrrolo[2,3-b]pyridine-3-yl)-phenol and 3.10 g of para-toluenesulfonyl chloride were dispersed in 400 ml of toluene at 45° C. 45 ml of 50% aqueous solution of KOH and 1.5 ml of 40% aqueous solution of tetra-n-butylammonium hydroxide were added and the resulting mixture stirred vigorously at ambient temperature for 6 h. The resulting mixture was diluted with 100 ml of a saturated aqueous solution of sodium bromide, the phases separated and the aqueous layer extracted three times with toluene. The combined organic phases were washed with a 2 M aqueous solution of sodium hydroxide, dried over sodium sulfate and evaporated. The crude was crystallized from ethanol containing 10% v/v of toluene to afford 3.22 g (5.29 mmol, 55% yield) of toluene-4-sulfonic acid 4-[5-bromo-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-yl]-phenyl ester as ivory crystalline needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361763B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-9faca65eb62741fa9acde4b24d50515d |
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| Source note | uspto-grants-2008_04 |
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