HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174516Generated: October 25, 2026
1-Methoxynaphthalene → 4-Methoxynaphthalene-1-sulfonyl chloride
https://huagongshe.com/reaction/1174516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methoxynaphthalene | HCID 16668 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methoxynaphthalene-1-sulfonyl chloride | HCID 16775501 | 93% |
Reaction Steps
To a cooled (0° C.) solution of 1-methoxy naphthalene (5 cm3, 34.5 mmol) in dichloromethane (20 cm3) was added, over a 10 minute period, chlorosulfonic acid (4.6 cm3, 69.0 mmol). Following this addition, phosphorus pentachloride (7.2 g, 34.5 mmol) was added and the reaction was maintained at 0° C. for a further 45 min. The reaction was then quenched by pouring onto ice/water (50 cm3), and allowed to warm to room temperature. Further dichloromethane (40 cm3) was added and the solution was transferred to a separating funnel, where the organic layer was collected and washed with saturated aqueous sodium chloride solution (70 cm3) and dried over sodium sulfate. The solvent was then evaporated under reduced pressure to afford title compound (8.23 g, 32.1 mmol; 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838518B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-ff5fed65b705401ea351cd4fc666e559 |
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| Source note | uspto-grants-2010_11 |
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