HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39163Generated: October 29, 2026
Acetonitrile → 3-Bromo-4-(cyanomethyl)phenylcyclopropane carboxamide
https://huagongshe.com/reaction/39163
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(benzo[d][1,3]dioxol-5-yl)-N-(3-bromo-4-(hydroxymethyl)phenyl)cyclopropanecarboxamide | HCID 59206247 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-4-(cyanomethyl)phenylcyclopropane carboxamide | HCID 86645850 | 46% |
Reaction Steps
1-(Benzo[d][1,3]dioxol-5-yl)-N-(3-bromo-4-(hydroxymethyl)phenyl)cyclopropane-carboxamide (1.08 g, 2.78 mmol), methanesulfonyl chloride (0.24 mL, 3.1 mmol), and N,N-diisopropylethylamine (0.72 mL, 4.1 mmol) were dissolved in acetonitrile (27 mL) at 25° C. After complete dissolution, KCN (450 mg, 6.95 mmol) was added and the reaction was stirred for 14 d. The reaction was diluted with dichloromethane (25 mL) and washed with water (25 mL). The organic extracts were dried over Na2SO4 and evaporated. The crude product was purified by chromatography on silica gel (eluting with 0-100% ethyl acetate in hexanes) to afford 1-(benzo[d][1,3]dioxol-5-yl)-N-(3-bromo-4-(cyanomethyl)phenylcyclopropane carboxamide (514 mg, 46%). ESI-MS m/z calc. 398.0, found 399.1 (M+1)+; retention time 3.24 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524767B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-81c683f1e96a4aeca24c939b9be25311 |
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| Source note | uspto-grants-2013_09 |
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