HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372019Generated: October 30, 2026
Water → N-Butyl-N-(1-methyl-1H-pyrrol-2-yl)acetamide
https://huagongshe.com/reaction/372019
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(1-Methyl-1H-pyrrol-2-yl)acetamide | HCID 14489757 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Butyl-N-(1-methyl-1H-pyrrol-2-yl)acetamide | HCID 20353305 | 83% |
Reaction Steps
N-(1-Methylpyrrol-2-yl)acetamide (3.20 g, 0.0231 mol) in dry dimethylformamide was maintained at a temperature less than 0° C, with stirring under nitrogen, during the slow addition of 50% sodium hydride/oil (1.11 g, 0.0231 mol). After the addition, the mixture was stirred at 0° C. for 30 minutes and then the temperature allowed to rise to 15° C. when n-butyl iodide (8.50 g, 0.0461 mol) was added. The mixture was stirred at room temperature overnight and then poured into water (200 ml) and the mixture extracted with ether (4 × 50 ml). The combined extracts were washed with water (3 × 50 ml) and dried over magnesium sulphate. The solvent was removed in vacuo and the resulting oil distilled to give a colourless oil 3.72 g (83%) b.p. (airbath) 100° C/0.4 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04088773 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-4fdd13a5cfd941c1a740dac186199ce8 |
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| Source note | uspto-grants-1978_05 |
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