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HRID 2372962作成日:2026年10月26日

Mercuric cyanide → 4-trifluoromethylphenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranoside

https://huagongshe.com/reaction/2372962

反応式

関与物質

役割名称HCID仕込み量
反応物Mercuric cyanideHCID 11591—
反応物4-(Trifluoromethyl)thiophenolHCID 136653—
反応物2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
生成物4-trifluoromethylphenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranosideHCID 1479534140%

反応手順

If the procedure described in Preparation I is followed starting from 5.58 g (32.10-3 mol) of 4-trifluoromethylbenzenethiol, 8.87 g (35.10-3 mol) of mercuric cyanide, Hg(CN)2, and 12.3 g (35.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide, 6.2 g (yield: 40%) 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-1da38ccf17f44fe1918c002c71af7f11
出典メモuspto-grants-1992_03