HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522503Generated: October 28, 2026
2-Furancarbonyl chloride → HCID 58526528, compound
https://huagongshe.com/reaction/522503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Furancarbonyl chloride | HCID 68242 | — |
| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58526528 | HCID 58526528 | 71% |
Reaction Steps
4,6-Dichloropyrimidine 6 (149 mg, 1.0 mmol) in THF (2 mL) was added to a solution of TMPZnCl.LiCl (2) (1.3 M in THF, 0.85 mL, 1.1 mmol) at 25° C. and the reaction mixture was then stirred at this temperature for 45 min according to TP 2. CuCN.2LiCl (1.0 M solution in THF, 1.1 mL, 1.1 mmol) was slowly added at −20° C. and the reaction mixture was stirred at the same temperature for 30 min. Then, furan-2-carbonyl chloride (261 mg, 2.0 mmol) was dropwise added at −20° C. and the resulting mixture was allowed to warm up slowly to 25° C. overnight. The reaction mixture was quenched with a sat. aq. NH4Cl solution (30 mL), extracted with diethyl ether (5×30 mL) and dried over anhydrous Na2SO4. After filtration, the solvent was evaporated in vacuo. Purification by flash-chromatography (CH2Cl2/n-pentane 1:1) furnished 8b as a colourless solid (172 mg, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334237B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-4d488838323f4555a4e464aa7d882f50 |
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| Source note | uspto-grants-2016_05 |
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