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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086921Generated: October 29, 2026

2-Acetylthiophene → HCID 700447, compound

https://huagongshe.com/reaction/2086921

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AcetylthiopheneHCID 6920—
ReactantMorpholineHCID 8083—
Reactant2-ThenoylacetonitrileHCID 141853—
ReactantSulfurHCID 5362487—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 700447HCID 70044744%

Reaction Steps

The procedure of Example 1 was followed except that 2-acetylthiophene (Aldrich) was used in place of acetophenone to prepare the corresponding 2-(thiophene-2-carbonyl)acetonitrile (Steps A and B). 2-Butanone (Aldrich), 2-(thiophene-2-carbonyl)acetonitrile, morpholine, and sulfur were reacted according to the procedure of Step C, Example 1, to afford the desired compound. Yield: 44%; IR (KBr) cm−1: 3390, 3269, 1552, 1429, 1272, 852, 772; 1H NMR (CDCl3):δ1.86 (s, 3H), 2.17 (s, 3H), 5.78(bs, 2H), 7.07 (dd, 1H, J=3.8 and 4.8 Hz), 7.56 (dd, 1H, J=2.8 and 0.8 Hz), 7.58 (dd, 1H, J=5.0 and 0.8 Hz); orange solid, mp: 117-118° C. (petroleum ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727258B2
Source datasetuspto-grants-2004_04
ORD IDord-a1ed061d19634c20a617c9d45c4c12b8
Source noteuspto-grants-2004_04