HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006942Generated: October 31, 2026
4-(1,3-Dioxolan-2-yl)benzonitrile → HCID 22502706, compound
https://huagongshe.com/reaction/1006942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(1,3-Dioxolan-2-yl)benzonitrile | HCID 2778428 | — |
| Reactant | n-Methyl-2-methylthiophene-3-carboxamide | HCID 22503091 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22502706 | HCID 22502706 | 31.7% |
Reaction Steps
To a solution of N-methyl-2-methylthiophene-3-carboxamide (18.5 g) in tetrahydrofuran (350 ml) was dropwise added 2.5M n-butyl lithium (100 ml) at −70° C. The resulting solution was stirred at −70° C. for 1.5 hr, followed by the addition of a solution of 4-(1,3-dioxolan-2-yl)benzonitrile (20.9 g) in tetrahydrofuran (100 ml) at once. After the dry ice/acetone bath was removed, the reaction mixture was back to room temperature. Three hours later, an aqueous solution of saturated ammonium chloride was added thereto, and the organic layer was separated, washed with water and dried. The filtrate was concentrated, and the resulting solid was washed with ethyl acetate, tetrahydrofuran/ether and n-hexane in this order. The resulting solid was then dried, to give the title compound as white crystals (6.24 g, yield; 31.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790844B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-86482fc44feb42a6b9d5b970ebfb4391 |
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| Source note | uspto-grants-2004_09 |
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