HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931514Generated: November 2, 2026
Aluminium lithium hydride → 4-[3-(4-Bromophenyl)propyl]morpholine
https://huagongshe.com/reaction/931514
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 3-(4-Bromophenyl)-1-morpholinopropan-1-one | HCID 22179856 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[3-(4-Bromophenyl)propyl]morpholine | HCID 22179832 | 82% |
Reaction Steps
To a mixture of lithium aluminum hydride (4.4 g, 115.79 mmol, 2.00 equiv) in tetrahydrofuran (120 mL) maintained under nitrogen at −30° C. was added a solution of 3-(4-bromophenyl)-1-morpholinopropan-1-one (17.2 g, 57.91 mmol, 1.00 equiv) in tetrahydrofuran (80 mL) dropwise with stirring. The resulting solution was stirred at −30° C. for 30 min and at room temperature for 2 h. The reaction was quenched by the sequential addition of 4.4 mL of water, 13 mL of 15% aqueous sodium hydroxide solution and 4.4 mL of water. The solid was removed by filtration and the filtrate was extracted with 1×350 mL of ethyl acetate. The organic layer was washed with 2×50 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum to afford 13.5 g (82%) of 4-(3-(4-bromophenyl)propyl)morpholine as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296732B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-5d65964132ca478395b2a84eec84562f |
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| Source note | uspto-grants-2016_03 |
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