HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650248Generated: October 29, 2026
Acetyl chloride → HCID 21714057, compound
https://huagongshe.com/reaction/650248
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21714063 | HCID 21714063 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21714057 | HCID 21714057 | — |
Reaction Steps
1-Allyl-5-amino-6-oxo-2-phenyl-1,6-dihydropyrimidine hydrochloride was dissolved in tetrahydrofuran (27 ml) and triethylamine (1.16 ml, 8.33 mmol), and acetyl chloride (0.284 ml, 3.99 mmol) was added to it under cooling on ice, and the mixture was stirred at 0° C. for 30 minutes and at room temperature for 2 hours. After saturated aqueous sodium bicarbonate was added, the reaction solution was extracted with ethyl acetate, and it was washed with saturated saline. After dried over anhydrous sodium sulfate, the organic layer was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/2) whereby the title compound (617 mg, 69%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06271238B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-a2747ea284f34f46b162a8d7a2a1ee09 |
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| Source note | uspto-grants-2001_08 |
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