Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532422Generated: October 30, 2026

Sulfuric Acid → Methyl 5-bromo-3-nitrothiophene-2-carboxylate

https://huagongshe.com/reaction/532422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDichloromethaneHCID 6344—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-nitrothiophene-2-carboxylateHCID 11137855—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 5-bromo-3-nitrothiophene-2-carboxylateHCID 57618723—

Reaction Steps

Sulfuric acid (98% strength; 12 mL) was added to a solution of 3-nitrothiophene-2-carboxylic acid methyl ester (Barker et al., Synth. Commun. 1995, 25, 3729; 20.8 g) in trifluoroacetic acid (60 mL). At 0° C., N-bromosuccinimide (21.9 g) was added in portions over a period of 45 minutes. After a further 30 minutes, the mixture was warmed to room temperature and poured into ice-water. The organic phase obtained by extraction with dichloromethane was dried over magnesium sulfate and concentrated. The residue was purified by chromatography on silica gel. The product with the molecular weight of 266.07 (C6H4BrNO4S) was obtained in this way; MS (ESI): 266 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853208B2
Source datasetuspto-grants-2014_10
ORD IDord-ee92f664e879400481565ff939d28110
Source noteuspto-grants-2014_10