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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627756Generated: October 26, 2026

Triethylamine → 3-(4-Methylbenzoyl)thiophen-2-amine

https://huagongshe.com/reaction/1627756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,4-Dithiane-2,5-diolHCID 98330—
Reactant3-(4-Methylphenyl)-3-oxopropanenitrileHCID 522513—
SolventEthanolHCID 702—
Product3-(4-Methylbenzoyl)thiophen-2-amineHCID 859626130.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 4-methylbenzoylacetonitrile (0.325 g; 2.042 mmol) and p-dithiane-2,5-diol (0.155 g; 1.018 mmol) in ethanol (4.3 mL) cooled at 0° C. was added triethylamine (0.283 mL; 2.042 mmol). After 10 min at room temperature, the reaction mixture was heated under reflux for 2 h. After cooling to room temperature, the reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over sodium sulphatesulphate, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel using a gradient of ethyl acetate (10-25%) in heptane to afford the title compound (0.288 g; 65%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785638B2
Source datasetuspto-grants-2014_07
ORD IDord-d5fc8a55d4d84a2daa06bb9f151e5ed1
Source noteuspto-grants-2014_07