HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515154Generated: October 29, 2026
Morpholine → 2-(Ethylsulfonyl)-6-methyl-4-morpholin-4-yl-benzonitrile
https://huagongshe.com/reaction/515154
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-2-(ethylsulfonyl)-6-methyl-benzonitrile | HCID 86699731 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-(Ethylsulfonyl)-6-methyl-4-morpholin-4-yl-benzonitrile | HCID 86699730 | 96% |
Reaction Steps
4-Chloro-2-(ethylsulfonyl)-6-methyl-benzonitrile (0.43 g, 1.77 mmol), morpholine (0.46 ml, 5.31 mmol) and potassium carbonate (0.32 g, 2.30 mmol) are taken up in N-methyl-2-pyrrolidone (3 ml) in a sealed tube and the resulting mixture is heated at 150° C. for 2 d. The mixture is then diluted with water (6 ml) and extracted with ethyl acetate (3×10 ml). The organic layer is washed with water (2×10 ml), brine (20 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 25% ethyl acetate/hexane) to yield 2-(ethylsulfonyl)-6-methyl-4-morpholin-4-yl-benzonitrile (0.50 g, 1.70 mmol, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108936B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-a60b109d75a84e7897526f06d9a3cc17 |
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| Source note | uspto-grants-2015_08 |
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