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HRID 1496821作成日:2026年10月23日

2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactopyranose → 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactitol

https://huagongshe.com/ja/reaction/1496821

反応式

関与物質

役割名称HCID仕込み量
反応物2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactopyranoseHCID 2734154—
反応物Sodium borohydrideHCID 4311764—
溶媒EthanolHCID 702—
生成物2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactitolHCID 1000752491%

反応手順

2,3,4,6-Tetra-O-benzyl-D-galactopyranose (107 g) was dissolved in ethanol (0.6 L) and, whilst stiffing at 0° C., sodium borohydride (31 g) was added. After stiffing overnight TLC analysis indicated completion of the reaction. The ethanol solution was partitioned between water (3 L) and ether (1.5 L). The organic phase was dried (Na2SO4), filtered and concentrated. The resulting oil was purified by flash chromatography (gradient elution using 20→50% ethyl acetate/petroleum ether) and then crystallised from a mixture of ethyl acetate/petroleum ether to give 2,3,4,6-tetra-O-benzyl-D-galactitol (97 g, 91%) as a white solid. 1H NMR (CDCl3): δ 2.4 (1H, bs), 3.35 (1H, bs), 3.55 (2H, m), 3.8 (3H, m), 3.9 (2H, m), 4.1 (1H, m), 4.4-4.8 (8H, m, OCH2Ph), 7.2-7.4 (20H, m, ArH). Mass spectrum: m/z 543 (M+H)+565 (M+Na)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09199935B2
出典データセットuspto-grants-2015_12
ORD IDord-1d0e56e26a8c4f4a901849d8875b63cd
出典メモuspto-grants-2015_12