HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654999Generated: November 2, 2026
Acetyl chloride → HCID 178471607, compound
https://huagongshe.com/reaction/654999
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Methyl 4-ethoxycarbonyl-3-oxopentanoate | HCID 14348549 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178471607 | HCID 178471607 | — |
Reaction Steps
Methyl 4-ethoxycarbonyl-3-oxopentanoate (200 ml; 1.06 mmole) was dissolved in dry methanol (2.5 ml), and benzylamine (386 mg; 3.6 mmole) and molecular sieve 3A (0.3 g) were added thereto. A solution of acetyl chloride (170 mg; 2.17 mmole) in dry methanol (0.9 ml) was added to the resultant mixture, followed by allowing to stand at room temperature for 16 hours. Molecular sieve was removed by filtraton, and the filtrate was diluted with ethyl acetate, washed successively with a saturated sodium bicarbonate solution and water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was dissolved in toluene (2.5 ml). Gaseous ketene was introduced therein at room temperature. After completion of the reaction, the solvent was removed under reduced pressure, and the residue was purified by silica gel column chromatography to give methyl ethyl 2-acetyl-3-benzylamino-4-methyl-2-pentenedioate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05134231 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-faf2c9fc1d9a4143b6d40e546cdac883 |
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| Source note | uspto-grants-1992_07 |
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