HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629765Generated: November 1, 2026
Bromoacetyl bromide → HCID 40562710, compound
https://huagongshe.com/reaction/629765
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | (4R)-4-phenyl-1,3-oxazolidin-2-one | HCID 730425 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Acetone cardice | HCID 18522661 | — |
| Product | HCID 40562710 | HCID 40562710 | — |
Reaction Steps
A solution of (4R)-4-phenyl-1,3-oxazolidin-2-one (100 g, 613 mmol) in THF (2 L) under a nitrogen atmosphere was cooled to −78° C. in dry ice-acetone bath. To the stirred solution was added n-BuLi (337 mL, 2 M solution in cyclohexane, 675 mmol) dropwise over a period of 30 min, followed by the addition of 2-bromoacetyl bromide (123.7 g, 613 mmol) over 15 min. The resulting solution was stirred at 25° C. for 2 h. The reaction was quenched with aqueous NH4Cl (500 mL), and the mixture was extracted three times with EtOAc (3×1 L). The combined organic extracts were washed with water (500 mL) and brine (500 mL), dried (MgSO4), filtered, and the solvent was removed under reduced pressure to give the title compound as a brown solid. The crude product was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315475B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-37cdb8a0b6d24273b5162e730277bf67 |
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| Source note | uspto-grants-2016_04 |
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