HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516964Generated: October 26, 2026
Dichloromethane → 4-(4-Bromo-3-fluorobenzyl)morpholine
https://huagongshe.com/reaction/516964
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 4-Bromo-3-fluorobenzaldehyde | HCID 2783411 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | Ammonia | HCID 222 | — |
| Product | 4-(4-Bromo-3-fluorobenzyl)morpholine | HCID 53417818 | 66% |
Reaction Steps
A mixture of morpholine (0.215 ml, 2.46 mmol) and 4-bromo-3-fluorobenzaldehyde, available from Alfa Aesar, (500 mg, 2.46 mmol) was prepared in chloroform (8 ml) at room temperature and heated to 58-60° C. in a sealed tube for 1 h. The mixture was then cooled to room temperature and sodium triacetoxyborohydride (783 mg, 3.69 mmol) was added and the mixture heated again to 58-60° C. in a sealed tube for 12 h. The mixture was then allowed to cool to room temperature, diluted with water (4 ml), shaken vigorously and the mixture filtered through a phase separator and the filtrate concentrated in vacuo. The mixture was then purified by SCX-2 chromatography (Eluent: dichloromethane (2×10 ml), 10% methanol/dichloromethane (2×10 ml), methanol (2×10 ml), 7M NH3 in methanol/dichloromethane (2×10 ml) to afford 4-(4-bromo-3-fluorobenzyl)morpholine as a colourless oil (447 mg, 1.63 mmol, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115088B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-b04c39a32f78474e804a11fcc2e8dc71 |
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| Source note | uspto-grants-2015_08 |
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