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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTert-Butyl nitriteHCID 10906—
Reactant2-Amino-4-chloro-5-formyl-3-thiophenecarbonitrileHCID 2737612—
SolventDimethylformamideHCID 6228—
Product5-Formyl-4-chlorothiophene-3-carbonitrileHCID 1993534868%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740647B1
Source datasetuspto-grants-2004_05
ORD IDord-305eea2c6e2144cf9d61b01ea03bb2e8
Source noteuspto-grants-2004_05