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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1496821생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactopyranoseHCID 2734154—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
생성물2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactitolHCID 1000752491%

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09199935B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-1d0e56e26a8c4f4a901849d8875b63cd
출처 메모uspto-grants-2015_12