HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280833Generated: October 27, 2026
Methanesulfonyl chloride → Methyl 2-[(methanesulfonyl)oxy]-4-nitrobenzoate
https://huagongshe.com/reaction/280833
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Salicylic acid, 4-nitro-, methyl ester | HCID 139539 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Methyl 2-[(methanesulfonyl)oxy]-4-nitrobenzoate | HCID 23320160 | — |
Reaction Steps
Methyl 2-hydroxy-4-nitrobenzoate (19.7 g) was dissolved in 100 ml of chloroform and triethylamine (15 ml). The solution was kept at a temperature below 15° C., and methanesulfonylchloride (8.6 ml) was added dropwise. The solution was maintained at 50° C. for 1 hr, whereupon it was poured onto ice-hydrochloric acid and extracted with a total of 600 ml chloroform. The solution was dried with magnesium sulfate, treated with active carbon and evaporated. The product was recrystallized from methanol. Yield: 20 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04591584 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-e999d4d5001244278c3eb477e6871205 |
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| Source note | uspto-grants-1986_05 |
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