HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097021Generated: October 30, 2026
4-Nitrobenzenesulfonyl chloride → 4-Nitrobenzenesulfonic Acid 2-[3-(Tritylamino)phenyl]ethyl Ester
https://huagongshe.com/reaction/1097021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-[3-(Tritylamino)phenyl]ethanol | HCID 66770330 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Nitrobenzenesulfonic Acid 2-[3-(Tritylamino)phenyl]ethyl Ester | HCID 86646960 | 100% |
Reaction Steps
To a stirred solution of 2-[3-(tritylamino)phenyl]ethanol (5.00 g, 13.2 mmol) and triethylenediamine (2.22 g, 19.8 mmol) in DCM (52.7 mL) under nitrogen at 0° C. was added portion-wise p-nitrobenzenesulfonyl chloride (3.50 g, 15.8 mmol) over a period of 5 min. The resulting mixture stirred at 0° C. for 40 min and then saturated aqueous sodium bicarbonate solution (˜50 mL) was added. The mixture was stirred at room temperature for 10 min and then the layers were separated. The aqueous layer was extracted with DCM (2ט50 mL) and the combined organic layers were dried over sodium sulfate, filtered, and concentrated under reduced pressure to give the title compound (7.44 g, 100% yield) as an orange-yellow foamy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138345B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-aadb382e10734f85820bf0de496ef181 |
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| Source note | uspto-grants-2012_03 |
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