HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428706Generated: October 31, 2026
Methanesulfonyl chloride → 4-Nitrobenzyl methanesulfonate
https://huagongshe.com/reaction/1428706
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-Nitrobenzyl alcohol | HCID 69275 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Nitrobenzyl methanesulfonate | HCID 18924794 | 72.9% |
Reaction Steps
To a solution of (4-nitrophenyl)methanol (2 g, 13.06 mmol) in toluene (10 mL) was slowly added methane sulfonylchloride (1.21 mL, 15.67 mmol) at room temperature. The reaction mixture was heated to 80° C. for 4 h. TLC showed complete consumption of starting material. The reaction mixture was cooled to room temperature. The mixture was extracted with ethyl acetate and washed with water and brine. The extract was dried over magnesium sulfate and concentrated under reduced pressure. The crude was purified by column chromatography to give 4-nitrobenzyl methanesulfonate (2.2 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937092B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-7c882cb5e8844d5eae5059e6db5d9022 |
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| Source note | uspto-grants-2015_01 |
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