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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2399777Erstellt: 26. Oktober 2026

Diethyl Ether → Benzeneacetic acid, 4-chloro-alpha-methylene-, ethyl ester

https://huagongshe.com/reaction/2399777

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktDiethyl CarbonateHCID 7766—
EduktEthyl (4-chlorophenyl)acetateHCID 84177—
EduktMethionin ALHCID 446793—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
ProduktBenzeneacetic acid, 4-chloro-alpha-methylene-, ethyl esterHCID 18100594,3%

Reaktionsschritte

Metal sodium (1.5 g) was gradually added to ethanol (50 ml) at room temperature, followed by stirring for 5 minutes, and diethyl carbonate (8.9 ml, 73 mmol) was added thereto at room temperature. Further, a solution of ethyl 4-chlorophenylacetate (10 g) in ethanol (10 ml) was added dropwise thereto with stirring, and the stirring was continued for 2 hours. The reaction mixture was concentreated, and diethyl ether (150 ml) and 10% aqueous acetic acid (150 ml) were added to the residue for extraction. The aqueous layer was further washed with diethyl ether (50 ml). The combined organic layer was dried over magnesium sulfate and concentrated under reduced pressure. To the resulting residue were added water (25 ml) and 37% aqueous formaldehyde (8 ml) at room temperature, followed by vigorous stirring at room temperature. After addition of an aqueous solution (36 ml) of potassium carbonate (6.5 g) over 5 minutes, the mixture reaction was stirred for 4 hours and extracted with diethyl ether (100 ml×2). The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give a crude product of ethyl 4-chlorophenyl-α-methyleneacetate (yield, 10 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05451607
Quelldatensatzuspto-grants-1995_09
ORD IDord-b2b0129939c94941b5b2903cac702def
Quellennotizuspto-grants-1995_09