HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952843Generated: November 2, 2026
Sodium Carbonate → 5-(Aminomethyl)thiophene-3-carbonitrile
https://huagongshe.com/reaction/1952843
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 5-Formylthiophene-3-carbonitrile | HCID 12280009 | — |
| Reactant | 5-[(Hydroxyimino)methyl]-3-thiophenecarbonitrile | HCID 73851632 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(Aminomethyl)thiophene-3-carbonitrile | HCID 11051716 | 106.9% |
Reaction Steps
4-Cyanothiophene-2-carbaldehyde oxime 11.6 g (84.6 mmol) of 4-cyanothiophene-2-carbaldehyde were dissolved in 140 ml of methanol, and 12.3 g (116.1 mmol) of sodium carbonate were added. Then 6.5 [lacuna] (93.5 mmol) of hydroxylamine hydrochloride were added in portions while cooling at 15° C., and the mixture was stirred at 10° C. for 2 h. After addition of 80 ml of water, the reaction mixture was extracted five times with 50 ml of diethyl ether each time, the organic phase was dried over sodium sulfate, and the solvent was removed under reduced pressure to result in 12.5 g of the required product as yellow crystalline powder (96% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06114358 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-e51373be831a4b7cb49226545a6b0a86 |
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| Source note | uspto-grants-2000_09 |
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