HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582924Generated: November 2, 2026
Acetonitrile → 5-Formyl-4-chlorothiophene-3-carbonitrile
https://huagongshe.com/reaction/1582924
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 2-Amino-4-chloro-5-formyl-3-thiophenecarbonitrile | HCID 2737612 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Formyl-4-chlorothiophene-3-carbonitrile | HCID 19935348 | 68% |
Reaction Steps
35 g (325 mmol) of tert-butyl nitrite were added dropwise at room temperature to a solution of 53.0 g (250 mmol) of 2-amino-4-chloro-5-formylthiophene-3-carbonitrile (the synthesis of this compound is described in Patent DB 3738910) in 600 ml of a 1:1 mixture of acetonitrile and dimethylformamide, during which process the temperature of the reaction mixture rose from 20° C. to 37° C. and vigorous evolution of gas began. The mixture was cooled to 25° C. and stirred for 7 hours at room temperature, the black solution was concentrated on a rotary evaporator under a high vacuum, the residue was purified by column chromatography (eluant dichloromethane), and 29 g (68%) of the desired compound were obtained as yellow oil. 1H NMR (270 MHz, DMSO-d6): δ=9.1 (s, 1H), 10.0 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06740647B1 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-305eea2c6e2144cf9d61b01ea03bb2e8 |
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| Source note | uspto-grants-2004_05 |
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