HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809052Generated: October 31, 2026
Tert-Butyl nitrite → HCID 59542515, compound
https://huagongshe.com/reaction/1809052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | HCID 59542517 | HCID 59542517 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Product | HCID 59542515 | HCID 59542515 | 74.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362008B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-a52b88b72ca44c198552594e3edfdb6e |
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| Source note | uspto-grants-2013_01 |
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