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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2627생성일: 2026년 10월 26일

Benzene → Octyl 2,6-di-O-benzoyl-4-O-(4-O-acetyl-2,6-di-O-benzoyl-beta-D-galacto-pyranosyl)-3-O-(2,3,4-tri-O-benzyl-alpha-L-fucopyranosyl)-beta-D-glucopyranoside

https://huagongshe.com/reaction/2627

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물p-Toluenesulfonic acidHCID 6101—
반응물TriethylorthoaceateHCID 21875354—
반응물Octyl 2,6-di-O-benzoyl-3-O-(2,3,4-tri-O-benzyl-alpha-L-fucopyranosyl)-4-O-(2,6-di-O-benzoyl-beta-D-galactopyranosyl)-beta-D-glucopyranosideHCID 22868661—
용매TriethylamineHCID 8471—
생성물Octyl 2,6-di-O-benzoyl-4-O-(4-O-acetyl-2,6-di-O-benzoyl-beta-D-galacto-pyranosyl)-3-O-(2,3,4-tri-O-benzyl-alpha-L-fucopyranosyl)-beta-D-glucopyranosideHCID 2286866391.3%

반응 단계

Compound 22 (5 g) was dissolved a 1:1 mixture of benzene and triethylorthoacetate (110 mL), containing 4-toluenesulfonic acid (0.2 g), and the mixture was stirred for 1 h at room temperature. The acid was neutralized with triethylamine, and the mixture evaporated to dryness. The residue was dissolved in 80% aqueous acetic acid (75 mL) and stirred for 40 min at room temperature. The acetic acid was evaporated under diminished pressure and the last traces were removed by co-evaporation with toluene to yield 23 (4.7 g, 91.3%); [α]D, -4.5° (c 0.8, chloroform), t.l.c. (5:1 ethyl acetate-toluene). 13C NMR (CDCl3): δ170.98 (COCH3), 166.75, 166.33, 166.18, 165.07 (4×PhCO), 102.03, 101.08 (C-1, C-1'), 98.16 (C-1 fuc), 80.07, 78.23 (C-3, C-4), 74.69, 73.53, 73.24 (3×PhCH2), 70.66 [OCH2 (CH2)6 ], 63.23, 61.42 (C-6, C-6'), 32.25-23.14 [(CH2)6CH3 ], 21.20 (COCH3), 17.49 (C-6 fuc), and 14.63 (CH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728685
출처 데이터셋uspto-grants-1998_03
ORD IDord-794405d5658443eaa2988d9f4b124f36
출처 메모uspto-grants-1998_03