HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325043Generated: October 30, 2026
2-Chlorobenzenesulfonyl chloride → HCID 86584800, compound
https://huagongshe.com/reaction/325043
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chlorobenzenesulfonyl chloride | HCID 76187 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86584801 | HCID 86584801 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86584800 | HCID 86584800 | 62% |
Reaction Steps
2-Chlorobenzenesulfonyl chloride (0.225 g; 1.06 mmol) was added to a cold solution (ice:water temperature) of 3-[2-(4-cyanophenyl)ethoxy]-5-methyl-phenylaminoacetic acid, ethyl ester (0.30 g; 0.88 mmol; from step (i) above) in pyridine (10 mL). After 2 hours stirring the temperature was allowed to rise to ambient. After 4 hours at this temperature more 2-chloro-benzenesulfonyl chloride (0.056 g; 0.26 mmol) was added and the mixture was left overnight. The mixture was then poured into aqueous saturated NaHCO3 and extracted twice with Et2O. The combined ether phases where washed with HCl/aq (2M), H2O and brine, dried (MgSO4) and the solvent removed in vacuo. The residue was purified by flash chromatography (SiO2; EtOAc:heptane (1:3)) to give 0.28 g (62%) of the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06221898B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-0b7a0c4e7c8147acb4d8af2c92ba8d43 |
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| Source note | uspto-grants-2001_04 |
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