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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809052Generated: October 31, 2026

Tert-Butyl nitrite → HCID 59542515, compound

https://huagongshe.com/reaction/1809052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
ReactantHCID 59542517HCID 59542517—
CatalystCupric ChlorideHCID 24014—
ProductHCID 59542515HCID 5954251574.8%

Reaction Steps

2-Amino-5-(2,2,2-trifluoro-ethyl)-thiophene-3-carboxylic acid ethyl ester (1.76 g, 6.96 mmol) was added to a suspension of t-butyl nitrite (10.4 mmol) and copper (II) chloride (26.8 mmol) in IMS (50 mL). The reaction mixture was stirred for 1.5 hours then quenched with saturated aqueous ammonium chloride (7 mL). The solvent was removed under vacuum and the residue partitioned between DCM and water. The organic solution was separated and dried over magnesium sulphate, filtered and the solvent evaporated. The product was purified by column chromatography on silica, eluting with 0%-35% t-butylmethylether in cyclohexane. The fractions containing the desired product were concentrated under vacuum to give the title compound (1.24 g). 1H NMR (400 MHz, CHCl3-d): δ 8.05 (s, 1H), 7.45 (s, 1H), 4.3 (q, 2H), 3.6 (q, 2H), 1.37 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362008B2
Source datasetuspto-grants-2013_01
ORD IDord-a52b88b72ca44c198552594e3edfdb6e
Source noteuspto-grants-2013_01