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HRID 2372955作成日:2026年10月25日

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

https://huagongshe.com/reaction/2372955

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-thioxylopyranosyl bromideHCID 11382683—
触媒ZincchlorideHCID 3007855—
触媒Silver imidazolateHCID 10931941—
溶媒AcetonitrileHCID 6342—
生成物4-cyanophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranosideHCID 1479533217%

反応条件

温度50 °C

反応手順

A suspension of 625 mg (1.76.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-D-xylopyranosyl bromide, 200 mg (1.48.10-3 mol) of 4-mercaptobenzonitrile and a 400 pm molecular sieve in 10 ml of acetonitrile is stirred in the presence of 605 mg (4.4.10-3 mol) of zinc chloride and 310 mg (1.8.10-3 mol) of silver imidazolate, in the absence of light, under an inert atmosphere. After heating at 50° C. for 3 h, the reaction mixture is filtered on Celite® in ethyl acetate. The filtrate is washed with a 1N solution of hydrochloric acid, water, a 1N solution of sodium hydroxide, water and finally a saturated solution of sodium chloride, dried over magnesium sulfate and evaporated under reduced pressure. After purification by chromatography on silica gel using a hexane/ethyl acetate mixture (3/1 v/v) as the eluent, and precipitation in ether, 100 mg (yield: 17%) of the expected product are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05101048
出典データセットuspto-grants-1992_03
ORD IDord-298f74cecbda45faaad853afc144fd2e
出典メモuspto-grants-1992_03