HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985833Generated: October 26, 2026
Ethanol → 3-(4-Hydroxybutylsulfanyl)benzylamine
https://huagongshe.com/reaction/1985833
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 3-(4-Acetoxybutylsulfanyl)benzonitrile | HCID 23143864 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Hydroxybutylsulfanyl)benzylamine | HCID 23143869 | 34.6% |
Reaction Steps
Lithium aluminum hydride (0.20 g) was suspended in tetrahydrofuran (15 mL). To the mixture was added 3-(4-acetoxy-butylsulfanyl)benzonitrile (0.75 g) under ice-cooling. The mixture was stirred at 60° C. for 2 hours, and the mixture was cooled under ice-cooling. To the reaction mixture were added dropwise ethanol and water successively, and then added diethyl ether. To the reaction mixture was added anhydrous sodium sulfate, and the insoluble material was removed by filtration. The filtrate was concentrated under reduced pressure to give the title compound (0.22 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07547680B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-2125763121bf4254a05e3b1588a41eb4 |
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| Source note | uspto-grants-2009_06 |
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