HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223238Generated: October 30, 2026
4-Nitrobenzenesulfonyl chloride → HCID 12669330, compound
https://huagongshe.com/reaction/223238
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Reactant | HCID 12669329 | HCID 12669329 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 12669330 | HCID 12669330 | 32% |
Reaction Steps
To a mixture of 3.00 g (10.6 mmoles) of 2-[(1,3,4,5-tetrahydro-7,8-dimethoxy-2-benzoxepin-1-yl)methoxy]ethanol and 1.63 ml (11.7 mmoles) of triethylamine is added 2.59 g (11.7 mmoles) of p-nitrobenzenesulfonyl chloride. The reaction mixture is stirred at room temperature for 1 hour and then heated at 50° for 30 minutes. To this is added an additional 0.5 g of p-nitrobenzenesulfonyl chloride and 0.5 ml of triethylamine. After stirring at room temperature for 30 minutes, the reaction mixture is extracted with aqueous sodium bicarbonate and brine. The organic layer is filtered through sodium sulfate and taken to dryness. The residue is chromatographed on silica gel using 1% methanol methylene chloride as eluant to give 1.56 g (32%) 2-[(1,3,4,5-tetrahydro-7,8-dimethoxy-2-benzoxepin-1-yl)methoxy]ethyl 4-nitrobenzene sulfonate. The nmr spectrum was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04352805 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-abac392004e94307ba5509ef13557cc7 |
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| Source note | uspto-grants-1982_10 |
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