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HRID 851673作成日:2026年10月25日

Hydrochloric Acid → 2-Carboxyethyl 2,3,4,6-tetra-O-acetyl-1-thio-alpha-D-mannopyranoside

https://huagongshe.com/reaction/851673

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Propanoic acid, 3-iodo-HCID 8856—
反応物Potassium CarbonateHCID 11430—
反応物Potassium MetabisulfiteHCID 28019—
反応物2-S-(2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranosyl)-2-thiopseudourea hydrobromideHCID 22823287—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物2-Carboxyethyl 2,3,4,6-tetra-O-acetyl-1-thio-alpha-D-mannopyranosideHCID 2352446899.1%

反応手順

A mixture of 2-S-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2-thiopseudourea hydrobromide (1) (90 g, 0.185 mol), freshly crystallized 3-iodopropionic acid (37 g, 0.199 mol), potassium carbonate (29.6 g, 0.215 mol), and potassium metabisulfite (37 g, 0.167 mol) in acetone (150 ml) and water (150 ml) is stirred for 45 minutes at room temperature. Hydrochloric acid (5%, 700 ml) and chloroform (700 ml) are added to the mixture. The organic layer is separated and washed with water, dried, and evaporated in vacuo to an oil (80 g, quantitative yield) that is used, without further purification, for the preparation of 3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04386026
出典データセットuspto-grants-1983_05
ORD IDord-f801664b6ce441f7bbdbcc7aa63ecf90
出典メモuspto-grants-1983_05