Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054231Generated: November 1, 2026

Methyl 3-amino-2-thiophenecarboxylate → Methyl 3-nitrothiophene-2-carboxylate

https://huagongshe.com/reaction/1054231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
ReactantSodium TetrafluoroborateHCID 4343483—
ReactantSodium NitriteHCID 23668193—
CatalystCopperHCID 23978—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-nitrothiophene-2-carboxylateHCID 1113785563%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a stirring solution of methyl 3-aminothiophene-2-carboxylate (5 g, 31.8 mmol) in Conc. HCl (4.77 ml) was added aq. solution of sodium nitrite (2.195 g, 31.8 mmol) slowly at 0-5° C. Reaction mixture was stirred at 0-5° C. for 1 h. To this was added aq. solution of sodium tetrafluoroborate (5.24 g, 47.7 mmol) in one lot. After 30 min. precipitated product was filtered. The product was added to the stirring suspension of copper bronze (6.06 g, 95 mmol) and sodium nitrite (26.3 g, 382 mmol) in water (100 ml). Reaction mixture was stirred at 25° C. for 1 h. Reaction mixture was diluted with water and EtOAc and filtered through Hyflow bed. The organic layer was separated and distilled out to get crude product which was column purified using 0-5% EtOAC in hexane to get titled compound as light yellow solid in 63% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394300B2
Source datasetuspto-grants-2016_07
ORD IDord-6133b796f30b426dab1c686e7820c60b
Source noteuspto-grants-2016_07