HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877693Generated: October 30, 2026
Boron trifluoride etherate → 1-(furan-2-yl)cyclopropanaMine
https://huagongshe.com/reaction/1877693
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Furonitrile | HCID 69245 | — |
| Reactant | HCID 178461630 | HCID 178461630 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(furan-2-yl)cyclopropanaMine | HCID 56773733 | — |
Reaction Steps
To a solution of 2-furonitrile (5 g, 53.71 mmol, 1.0 eq) in dry THF under an argon atmosphere was added slowly titanium isopropoxide (18.9 ml, 64.4 mmol, 1.2 eq) at r.t. The reaction mixture was stirred for 15 min. A 1M solution of EtMgBr in THF (129 ml, 129 mmol, 2.4 eq) was added slowly via syringe to the mixture at 0° C. After addition, the reaction mixture was allowed to warm to r.t. and stirred at r.t. for 2 hour. BF3.Et2O (10.4 ml) was then added slowly to the mixture at 0° C. After the completion of addition, the reaction mixture was stirred at r.t. for 30 min. The reaction mixture was added with ice, and then with 10% NaOH solution slowly till the reaction mixture becomes basic. The mixture was extracted with EtOAc. The organic was washed with brine, dried over Na2SO4 and concentrated. The crude product was purified by silica gel (60-120) column chromatography using 35% EtOAc/Pet ether as eluent. Yield: 2.5 g (crude).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309558B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-912cc34b7fbb4c26a4c4d912313e46a1 |
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| Source note | uspto-grants-2012_11 |
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