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HRID 5994作成日:2026年10月24日

4-Thiobenzonitrile → 4-cyanophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranoside

https://huagongshe.com/ja/reaction/5994

反応式

関与物質

役割名称HCID仕込み量
反応物4-ThiobenzonitrileHCID 585058—
反応物2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
触媒Zinc OxideHCID 3007857—
溶媒TolueneHCID 1140—
溶媒AcetonitrileHCID 6342—
生成物4-cyanophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranosideHCID 1479533264%

反応条件

温度50 °C

反応手順

A suspension of 16.9 g (47.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide, 6 g (43.10-3 mol) of 4-mercaptobenzonitrile and 3.5 g (43.10-3 mol) of zinc oxide (ZnO) in 120 ml of anhydrous toluene and 120 ml of acetonitrile is stirred under an inert atmosphere, in the presence of a molecular sieve (1 mm), for 18 hours, at 50° C. After the reaction medium has been filtered on Celite® in ethyl acetate, the organic phase obtained is washed with a 1N solution of HCl twice, a 1N solution of sodium hydroxide and finally water, dried over magnesium sulfate and evaporated under reduced pressure. After precipitation in ether, 11.30 g (yield: 64%) of the expected product are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246961
出典データセットuspto-grants-1993_09
ORD IDord-c325c2e4bd414d69a18ffb5e8f24076c
出典メモuspto-grants-1993_09