HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516965Generated: October 30, 2026
Morpholine → 4-(4-Bromo-2,6-difluorobenzyl)morpholine
https://huagongshe.com/reaction/516965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 4-Bromo-2,6-difluorobenzaldehyde | HCID 2773290 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(4-Bromo-2,6-difluorobenzyl)morpholine | HCID 59392758 | 37% |
Reaction Steps
A mixture of 4-bromo-2,6-difluorobenzaldehyde, available from Sigma-Aldrich, (500 mg, 2.26 mmol) and morpholine (0.198 ml, 2.26 mmol) was prepared in chloroform (10 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 (719 mg, 3.39 mmol) was added and the mixture heated again to 58-60° C. in a sealed tube for 60 h. The mixture was allowed to cool down to room temperature and then washed with water (5 ml), filtered through a phase separator and concentrated in vacuo. Crude 1HNMR (CDCl3) suggested an 8:2 mixture of the desired amine to the imine product. After initial chromatography (1-5% methanol/dichloromethane) which did not separate products, mixture was purified by preparative HPLC to afford 4-(4-bromo-2,6-difluorobenzyl)morpholine as a colourless oil (247 mg, 0.85 mmol, 37%).
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-29cba3a5bfed4656ab314fc00e1531ad |
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| Source note | uspto-grants-2015_08 |
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