HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850960Generated: October 30, 2026
Methanol → 4-Hexadecylamino-2-formylthiophene
https://huagongshe.com/reaction/850960
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Hexadecylamino-2-cyanothiophene | HCID 13134991 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methylenechloride Hexane | HCID 21226440 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Hexadecylamino-2-formylthiophene | HCID 13134992 | — |
Reaction Steps
Di-isobutylaluminum hydride (14 ml., 25% solution in toluene) is added with stirring to a solution of 2.9 g. of 4-hexadecylamino-2-cyanothiophene in toluene under a nitrogen atmosphere. The temperature rises during the addition and the reaction is then stirred for 1 hour. A solution of methanol in toluene (14 ml., 1:1) is added over 30 minutes and the mixture is poured into vigorously stirred ice-cold aqueous sulfuric acid (125 ml., 5%). After 10 minutes diatomaceous earth (7.5 g.) is added, the mixture filtered and the organic layer separated. The aqueous solution is extracted twice with toluene (25 ml.) and the combined organic layers are washed with aqueous sodium bicarbonate, dried over magnesium sulfate, decolorized with charcoal, filtered and evaporated in vacuo to give crude product. The product is obtained by recrystallization from dichloromethane-hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04382143 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-b43857b864a644fa9285a34a9ebf5612 |
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| Source note | uspto-grants-1983_05 |
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