HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335221Generated: October 29, 2026
Boron trifluoride → HCID 66995201, compound
https://huagongshe.com/reaction/335221
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | 2-Pyrrolidone | HCID 12025 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66995201 | HCID 66995201 | 16.4% |
Reaction Steps
2-Pyrrolidinone (4.47 g, 52.5 mmol) was mixed with THF (25 mL) and cooled to −78° C. Butyllithium (1.6 M in hexanes) (32.8 mL, 52.5 mmol) was added slowly then and the mixture was agitated for 10 minutes. Boron trifluoride ethereate (6.59 mL, 52.5 mmol) was added dropwise, followed by dropwise addition of epichlorohydrin (4.11 mL, 52.5 mmol). The resulting mixture was allowed to warm up overnight, then cooled and quenched with saturated sodium bicarbonate solution, and extracted 3 times with ethyl acetate. The extracts were washed with brine, dried and evaporated to give ˜4 g of crude oil. The crude oil was purified by chromatography on silica gel, eluting with 1-2% methanol/dichloromethane, to provide the title compound (1.53 g, 16.4% yield) as clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883828B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-4db4165df14b466aab7523621af2dbd6 |
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| Source note | uspto-grants-2014_11 |
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