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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654999Generated: November 2, 2026

Acetyl chloride → HCID 178471607, compound

https://huagongshe.com/reaction/654999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantBenzylamineHCID 7504—
ReactantMethyl 4-ethoxycarbonyl-3-oxopentanoateHCID 14348549—
SolventMethanolHCID 887—
ProductHCID 178471607HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05134231
Source datasetuspto-grants-1992_07
ORD IDord-faf2c9fc1d9a4143b6d40e546cdac883
Source noteuspto-grants-1992_07