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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSalicylic acid, 4-nitro-, methyl esterHCID 139539—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductMethyl 2-[(methanesulfonyl)oxy]-4-nitrobenzoateHCID 23320160—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04591584
Source datasetuspto-grants-1986_05
ORD IDord-e999d4d5001244278c3eb477e6871205
Source noteuspto-grants-1986_05