Anisacril Chemische Eigenschaften,Einsatz,Produktion Methoden

Originator

SCF 16046,Smith Kline

Manufacturing Process

A solution of Grignard reactive (prepared from 247 g of o-bromoanisole and 31.6 g of magnesium in 1500 ml of ether) is added dropwise to a solution of 91 g of diphenyl pyruvic acid in ether. The mixture is refluxed for 2 hours. After cooling to the reaction mixture is added 5% hydrochloric acid and the product is extracted with 5% solution of sodium hydroxide. α-(o-Anisyl)-β,β- diphenyl lactic acid is precipitated by addition of concentrated hydrochloric acid; yield 62 g, melting point 194-195°C.
4 g of α-(o-anisyl)-β,β-diphenyl lactic acid is heated at 210-215°C for 10-15 min. The α-(o-anisyl)-β,β-diphenyl acrylic acid is recrystallized from benzene, yield 2.85 g (74%), melting point 195-196°C.

Therapeutic Function

Anorexic, Antihyperlipidemic

Anisacril Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

Anisacril Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
Lanospharma Laboratories Co.,Ltd	--	sales@lanospharma.com	China	6329	56

5129-14-6()Verwandte Suche:

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• Anisacril
• 2-(2-methoxyphenyl)-3,3-di(phenyl)acrylic acid
• 2-(2-methoxyphenyl)-3,3-di(phenyl)prop-2-enoic acid
• 2-(2-methoxyphenyl)-3,3-diphenylacrylic acid(WXG02282)
• α-(o-Anisyl)-β,β-diphenylacrylsaeure
• Benzeneacetic acid, α-(diphenylmethylene)-2-methoxy-
• 5129-14-6