HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592834Generated: October 30, 2026
Carbon tetrabromide → HCID 58610157, compound
https://huagongshe.com/reaction/1592834
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 58610153 | HCID 58610153 | — |
| Reactant | HCID 58610189 | HCID 58610189 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58610157 | HCID 58610157 | 34% |
| Product | HCID 58610179 | HCID 58610179 | — |
Reaction Steps
A solution of carbon tetrabromide (3.3 g, 9.96 mmol) in dichloromethane (4 ml) was added dropwise over 5 min to a stirred solution of (R)-[3-fluorophenyl][(2R)-4-benzylmorpholin-2-yl]methanol and (S)-[3-fluorophenyl][(2S)-4-benzylmorpholin-2-yl]methanol (2.0 g, 6.64 mmol) and triphenylphosphine (2.61 g, 9.96 mmol) in dichloromethane (40 ml) at room temperature under nitrogen. After 30 min, the reaction solution was washed with saturated aqueous sodium bicarbonate (50 ml). The dichloromethane layer was dried, filtered and evaporated to a red liquid (8.5 g). Trituration with diethyl ether (40 ml) crystallised triphenylphoshine oxide that was then removed by filtration. The filtrate was evaporated to a yellow oil and was purified by chromatography on silica eluting with ethyl acetate:hexane 20:80 to give a colourless oil of (2R)-2-[(S)-bromo(3-fluorophenyl)methyl]-4-benzylmorpholine and (2S)-2-[(R)-bromo(3-fluorophenyl)methyl]-4-benzylmorpholine (0.811 g, 34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07294623B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-b9ac7801d3e64fa282406bed553f8429 |
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| Source note | uspto-grants-2007_11 |
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