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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654986Generated: October 30, 2026

Acetyl chloride → HCID 178457297, compound

https://huagongshe.com/reaction/654986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantAllylamineHCID 7853—
ReactantHCID 14348494HCID 14348494—
SolventMethanolHCID 887—
ProductHCID 178457297HCID 178457297—

Reaction Conditions

Temperature40 °C

Reaction Steps

Methyl 3-oxo-4-methyl-5-benzyloxypentanoate (1.11 g; 4.43 mmole) was dissolved in dry methanol (5 ml), allylamine (1.26 g) and molecular sieve 3A (0.6 g) were added thereto and then a solution of acetyl chloride (1.04 g; 13.3 mmole) in dry methanol (2 ml) was added thereto with icecooling, followed by stirring at 40° C. for 12 hours. The molecular sieve was removed by filtration, and the filtrate was diluted with ethyl acetate. The reaction mixture was washed successively with a saturated sodium bicarbonate solution and an aqueous sodium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was dissolved in toluene (5 ml), and 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 2-acetyl-3-allylamino-4-methyl-5-benzyloxy-2-pentenoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05134231
Source datasetuspto-grants-1992_07
ORD IDord-0694dfa53ca34ae5b41ef2823b47ba3f
Source noteuspto-grants-1992_07