HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677344Generated: October 25, 2026
Bromoacetonitrile → (4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-acetonitrile
https://huagongshe.com/reaction/1677344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Ethyl-7-methyl-benzo[b]thiophen-5-ol | HCID 59598702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-acetonitrile | HCID 59598537 | 91.2% |
Reaction Steps
4-Ethyl-7-methyl-benzo[b]thiophen-5-ol (438 mg, 2 mmol) was dissolved in 10 ml DMF, and the reaction mixture was cooled to zero degrees C. Sodium hydride (66 mg, 3 mmol) was added and the reaction mixture was stirred 30 minutes at zero C. Bromoacetonitrile (170 ul, 3 mmol) was added, and the reaction mixture was stirred 10 minutes at zero degrees C., then allowed to warm to room temperature. The reaction was quenched after 1 hour at room temperature with water, diluted with ethyl acetate, washed with water, brine, and dried over magnesium sulfate. Solvent was removed in vacuo, and the residue chromatographed (10% ethyl acetate in hexanes) to give 422 mg of (4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-acetonitrile as an oil, 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008313B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-8cd33dfc8a3548d89f3015cfa00547d2 |
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| Source note | uspto-grants-2011_08 |
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