HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332095Generated: October 26, 2026
Triethylamine → 5-((3,6-dibromo-9H-carbazol-9-yl)methyl)oxazolidin-2-one
https://huagongshe.com/reaction/332095
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Dichloromethane ethylacetate | HCID 21226138 | — |
| Reactant | 1-amino-3-(3,6-dibromo-9H-carbazol-9-yl)propan-2-ol | HCID 46852671 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-((3,6-dibromo-9H-carbazol-9-yl)methyl)oxazolidin-2-one | HCID 58097198 | 92.2% |
Reaction Steps
A solution of triphosgene (0.0890 g, 0.300 mmol, 0.35 equiv) in 2 mL anhydrous CH2Cl2 was added dropwise to a solution of 1-amino-3-(3,6-dibromo-9H-carbazol-9-yl)propan-2-ol (0.3413 g, 0.857 mmol) and Et3N (0.1909 g, 1.886 mmol) in 1 mL CH2Cl2 under N2 atmosphere at 4° C. The reaction mixture was stirred for 15 min at 4° C. and then warmed to room temperature and stirred for 1 hour. CH2Cl2 was removed under vacuum. Saturated NH4Cl (5 mL) and 10 mL EtOAc was added to the residue and stirred for 20 min. Then the aqueous layer was separated and the organic layer was washed with water 2×10 mL. The combined aqueous layers were extracted with EtOAc, dried over anhydrous Na2SO4 and evaporated to afford the crude product, which was subjected to silica gel chromatography using CH2Cl2/EtOAc to afford 0.1173 g white solid, yield 20.0% over 2 steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877797B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-11b18c3494444d79b7a61a5b44b12f1a |
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| Source note | uspto-grants-2014_11 |
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