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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893538Generated: October 31, 2026

tert-Butyl 3-methyl-4-nitrobenzoate → tert-Butyl 4-amino-3-methylbenzoate

https://huagongshe.com/reaction/1893538

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-methyl-4-nitrobenzoateHCID 15283350—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-amino-3-methylbenzoateHCID 53432587106.2%

Reaction Steps

The compound (55.6 g, 234 mmol) obtained in step A was dissolved in an ethanol (200 ml)-tetrahydrofuran (100 ml) mixed solvent. Then, 10% palladium carbon (containing water) (10 g) suspended in ethanol (20 ml) was added. Under a hydrogen atmosphere and at room temperature, the reaction mixture was stirred for 5 hr, and filtered off through celite. The obtained solution was concentrated under reduced pressure to give the title compound (51.5 g) as a bistered oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513235B2
Source datasetuspto-grants-2013_08
ORD IDord-0e78d576db5141ff8e8ff2c5e463b656
Source noteuspto-grants-2013_08