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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914589Generated: November 1, 2026

Tert-Butyl nitrite → Ethyl 5-phenylthiophene-3-carboxylate

https://huagongshe.com/reaction/1914589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
Reactantethyl 2-amino-5-phenylthiophene-3-carboxylateHCID 638860—
CatalystCupric ChlorideHCID 24014—
SolventAmmonium ChlorideHCID 25517—
ProductEthyl 5-phenylthiophene-3-carboxylateHCID 5811032473.4%

Reaction Steps

Anhydrous copper (II) chloride (4 g, 0.03 mol) and tert-butyl nitrite (1.9 mL, 0.019 mol) were dissolved in IMS (100 mL) then treated with 2-amino-5-phenyl-thiophene-3-carboxylic acid ethyl ester (2 g, 8.097 mmol). After 30 minutes saturated aqueous ammonium chloride (20 mL) was added and the mixture left for a further 30 minutes. The resultant precipitate was filtered off and the filtrate was concentrated, washed with DCM, dried and concentrated to give a dark oil which was purified by column chromatography, eluting with 0-35% tert-butyl methyl ether in cyclohexane to afford 5-phenyl-thiophene-3-carboxylic acid ethyl ester as a yellow oil (1.38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614209B2
Source datasetuspto-grants-2013_12
ORD IDord-45f921380f6f41569b9950dd09a98e32
Source noteuspto-grants-2013_12