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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736362Generated: October 31, 2026

Allyl 2-methyl-6-nitrobenzoate → Allyl 2-amino-6-methylbenzoate

https://huagongshe.com/reaction/1736362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl 2-methyl-6-nitrobenzoateHCID 19432516—
SolventMethanolHCID 887—
ProductAllyl 2-amino-6-methylbenzoateHCID 1943248475%

Reaction Steps

Stannous chloride dihydrate (15.3 g, 67.8 mM) was suspended in methanol (25 ml), and a solution of allyl 2-methyl-6-nitrobenzoate (3.0 g, 13.6 mM) in methanol (5 ml) was added. The mixture was heated at reflux for 1 hour, cooled, and solvent removed. The residue was treated with ethyl acetate (100 ml), made basic with 880 ammonia and diluted with water (50 ml). The organic layer was decanted from the slurry of tin salts, which was extracted with two further portions of ethyl acetate. The combined organic extracts were washed with dilute ammonia, water, brine, and dried over MgSO4, to give allyl 2-amino-6-methylbenzoate as an oil (1.94 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541178
Source datasetuspto-grants-1996_07
ORD IDord-a6a9c3170fca4416b242b4f60ca75e49
Source noteuspto-grants-1996_07