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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436853Generated: November 1, 2026

Methanesulfonic Acid → 2-Methyl-3-nitrobenzyl alcohol

https://huagongshe.com/reaction/1436853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant2-Methyl-3-nitrobenzoic acidHCID 16096—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-3-nitrobenzyl alcoholHCID 90289—

Reaction Steps

500 ml of THF and 76.5 gm NaBH4 was stirred for 30 min. at ambient temperature. Solution of 2-Methyl-3-nitro benzoic acid in THF (250 g in 750 ml) was added and stirred for 0.5 hour at ambient temperature. Further, methanesulphonic acid (90 ml) was added to the reaction mixture and stirred until the completion of reaction. The reaction mixture is extracted with ethyl acetate by addition of Hydrochloric acid and product organic layer is separated out. Ethyl acetate is evaporated to give 2-Methyl-3-nitrobenzyl alcohol as yellow oil, which is further treated with cyclohexane and crystallized to give 2-Methyl-3-nitrobenzyl alcohol (Yield: ˜210 g., 84%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07619095B2
Source datasetuspto-grants-2009_11
ORD IDord-1d761842748b4b25815946e3b6b38806
Source noteuspto-grants-2009_11