HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225388Generated: October 25, 2026
2-Methoxyethane-1-sulfonyl chloride → HCID 86594616, compound
https://huagongshe.com/reaction/225388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyethane-1-sulfonyl chloride | HCID 13480221 | — |
| Reactant | HCID 22064584 | HCID 22064584 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86594616 | HCID 86594616 | — |
Reaction Steps
3-(2-Benzyl-2-aza-bicyclo[3.3.1]non-5-yl)-phenylamine (2.71 g, 8.84 mmol) stirred in pyridine (25 ml) at 0° C. was charged with 2-methoxy-ethanesulfonyl chloride (2.1 g, 13.26 mmol) dropwise causing a color change from yellow to bright orange. The reaction was allowed to warm to room temperature gradually and stirred 18 h. The reaction mixture was diluted with toluene and concentrated in vacuo. The residue was dissolved in CH2Cl2 and washed with saturated aqueous NaHCO3 solution (100 mL). The aqueous layer was extracted with CH2Cl2 (2×50 ml) and the organic layer was concentrated to an oil. This was dissolved in EtOAc which caused an oil to separate. The EtOAc layer was separated and washed with saturated aqueous NaHCO3 solution (100 mL). The aqueous layer was extracted with EtOAc (2×50 ml) and the combined organic layer was washed with saturated aqueous NaCl solution (50 ml), dried over Na2SO4, filtered and concentrated to a crude orange liquid (3.77 g, ˜100%). (TLC 75% EtOAc/hexanes Rf 0.48);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE040838E1 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-d2de0c9643b54223baee8050e9ef6cc5 |
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| Source note | uspto-grants-2009_07 |
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