HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779972Generated: November 1, 2026
2-(Chloromethyl)furan → HCID 22872533, compound
https://huagongshe.com/reaction/1779972
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Chloromethyl)furan | HCID 219520 | — |
| Reactant | (R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine | HCID 736066 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 22872533 | HCID 22872533 | — |
Reaction Steps
A 1.55M solution of butyllithium (6.45 ml, 10 mmol) in hexane was added by syringe to a stirred solution of (2R)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine (1.84 g, 10 mmol) in THF (50 ml) at -78° C. and the solution stirred for 1 hour at -78° C. A solution of 2-chloromethylfuran (1.3 g, 11 mmol) in THF (10 ml) was added gradually and the stirring continued overnight. The solvent was removed under reduced pressure, the residue dissolved in ethyl acetate (50 ml) and extracted with phosphate buffer (pH 7). The water phase was extracted twice with ethyl acetate (2×20 ml ). The organic layer was dried (MgSO4), solvent evaporated under reduced pressure and the residue purified by flash chromatography (diethyl ether/hexane 15/1, silica gel).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05629293 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-411496d5ddec4c59b767540a8c55ee01 |
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| Source note | uspto-grants-1997_05 |
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