HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324619Generated: October 30, 2026
Boron tribromide → N-[2-[(1S)-5-Bromo-2,3-dihydro-6-hydroxy-1H-inden-1-yl]ethyl]propanamide
https://huagongshe.com/reaction/324619
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 11012817 | HCID 11012817 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[2-[(1S)-5-Bromo-2,3-dihydro-6-hydroxy-1H-inden-1-yl]ethyl]propanamide | HCID 11066924 | 94.1% |
Reaction Steps
A solution of (S)-N-[2-(5-bromo-6-methoxyindan-1-yl)ethyl]propionamide (56.7 g, 174 mmol.) in dichloromethane (400 mL) was cooled to −30° C. To the solution was added dropwise slowly boron tribromide (95.8 g, 382 mmol.). The reaction mixture was stirred for 30 minutes while keeping at temperatures ranging from −20 to −15° C. The reaction mixture was poured into ice-water, which was stirred for further 10 minutes at room temperature. The organic matter was extracted with ethyl acetate. The extract solution was washed with a saturated aqueous saline solution and water, which was dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The residue was purified by means of silica gel column chromatography (ethyl acetate) to afford the title compound (yield 51.12 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06218429B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-bcbbeee576b149d28013ab89cab31c49 |
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| Source note | uspto-grants-2001_04 |
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