HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243497Generated: October 29, 2026
Aluminium lithium hydride → 4-[3-(2,4-dimethyl-1H-pyrrol-3-yl)-propyl]-morpholine
https://huagongshe.com/reaction/1243497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 3-(2,4-dimethyl-1H-pyrrol-3-yl)-1-morpholin-4-yl-propan-1-one | HCID 21925755 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[3-(2,4-dimethyl-1H-pyrrol-3-yl)-propyl]-morpholine | HCID 21925716 | 79.1% |
Reaction Steps
To a suspension of lithium aluminum hydride (2.67 g, 70 mmol) in tetrahydrofuran (100 ml) was added dropwise a solution of 3-(2,4-dimethyl-1H-pyrrol-3-yl)-1-morpholin-4-yl-propan-1-one (13.84 g, 59 mmol) in tetrahydrofuran (50 ml). The reaction mixture was stirred at 80° C. for 1 hour and cooled ins an ice bath. Ice was added to the reaction mixture slowly until gas evolution ceased. A few drops of 2N sodium hydroxide were added and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was then extracted with ethyl acetate, dried over anhydrous sodium sulfate and concentrated to give 10.37 g (79%) of 4-[3-(2,4-dimethyl-1H-pyrrol-3-yl)-propyl]-morpholine as a light brown oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119090B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-3c158734bf6d47d1ae5be013041997da |
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| Source note | uspto-grants-2006_10 |
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