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HRID 704465作成日:2026年10月25日

p-Toluenesulfonic acid → Toluenesulfonate

https://huagongshe.com/reaction/704465

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Sulfosalicylic AcidHCID 7322—
反応物TriphenylphosphineHCID 11776—
溶媒MethanolHCID 887—
生成物ToluenesulfonateHCID 3424274—
生成物2-SulfooxybenzoateHCID 21874451—

反応条件

温度0 °C

反応手順

In a preferred embodiment, a mixture containing an 11a-halo-6-deoxy-6-demethyl-6-methylenetetracycline. preferably the p-toluene sulfonate of 11a-chloro methacycline; bis(triphenylphosphine)(hydroxylamine hydrochloride) dichloro rhodium (II) or its O-alkyl derivative complex, preferably hydroxylamine hydrochloride complex; and a tertiary phosphine, preferably triphenylphosphine, in methanol is subjected to agitation in a stainless steel autoclave, and hydrogenated at about 50° to 90° C. under a pressure between about 3 and 12 kg/cm2, prior to the termination of the reaction. Sulfosalicylic acid is added and the reaction mixture is cooled to about 0° C. for 2-4 hours. The alpha-6-deoxy-5-oxytetracyline sulfosalicylate, preferably doxycyline sulfosalicylate (or toluene sulfonate) thus obtained is filtered and washed with methanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04987242
出典データセットuspto-grants-1991_01
ORD IDord-9f3ad719ca1d48e0ab72c73a89429169
出典メモuspto-grants-1991_01