HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095106Generated: November 2, 2026
4-(3-Nitro-5-trifluoromethyl-benzoyl)-morpholine → 4-[3-Nitro-5-(trifluoromethyl)benzyl]morpholine
https://huagongshe.com/reaction/2095106
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(3-Nitro-5-trifluoromethyl-benzoyl)-morpholine | HCID 21954989 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[3-Nitro-5-(trifluoromethyl)benzyl]morpholine | HCID 21955005 | 38% |
Reaction Steps
To a solution of morpholin-4-yl-(3-nitro-5-(trifluoromethyl)phenyl)methanone (457 mg, 1.5 mmol) in THF (5 mL) was added dropwise a solution of borane tetrahydrofuran complex solution (3.1 mL, 3.1 mmol) at ambient temperature and the mixture was heated under reflux for 30 minutes, then cooled. The solvent was evaporated. Aqueous HCl (5 mL) was added and the resulting mixture was heated at 100° C. for 1 hour, then cooled and extracted with ether. The acidic aqueous layer was separated, basified to pH 8 with NaOH and extracted with ether. The ether solution was dried over anhydrous Na2SO4. Evaporation of ether provided 168 mg (0.57 mmol) of 4-(3-Nitro-5-trifluoromethylbenzyl)morpholine (38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445694B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-5942a123242a4d52a83e7fde969dd185 |
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| Source note | uspto-grants-2013_05 |
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