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HRID 219486作成日:2026年10月25日

Cyclohexanol, 2-((dimethylamino)methyl)-1-(3-methoxyphenyl)-, hydrochloride (1:1) → 2-((Dimethylamino)methyl)-1-(3-methoxyphenyl)cyclohexanol

https://huagongshe.com/reaction/219486

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclohexanol, 2-((dimethylamino)methyl)-1-(3-methoxyphenyl)-, hydrochloride (1:1)HCID 9971980—
溶媒WaterHCID 962—
生成物2-((Dimethylamino)methyl)-1-(3-methoxyphenyl)cyclohexanolHCID 5523—

反応条件

温度50 °C

反応手順

The Tramadol Resin Complex was prepared by first dissolving 500 g of tramadol HCl in 8 liters of purified water, and then slowly adding 1,345 g of AMBERLITE™ IRP-69 resin with continuous mixing. The dispersion was mixed for 4 hours and upon completion, allowed to settle before decanting the supernatant. The slurring/decanting process was repeated twice with sufficient amounts of purified water. The wet resin complex was then dried in a VWR™ convection oven maintained at 50° C. until moisture content was about 25%. KOLLICOAT™ SR-30D polymer (467 g) was then slowly added to the wet resin complex in a Hobart type mixer (Kitchen Aid) to form a uniform mass. The wet mass was again dried in a 50° C. VWR™ convection oven to the moisture content around 20%. The semi-dried granules were then milled through a 40 mesh screen using CO-MIL™ brand mill and continued drying under 50° C. until the moisture content was between 4-6%. The dried granules were then milled through a 40 mesh screen using CO-MIL™ brand mill.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202537B2
出典データセットuspto-grants-2012_06
ORD IDord-aa63ecade64345a090275a9ff374f6d6
出典メモuspto-grants-2012_06