4,6-O-芐叉-D-葡萄糖 基本信息
| 中文名稱 | 4,6-O-芐叉-D-葡萄糖 |
|---|---|
| 中文同義詞 | 4,6-O-芐叉-D-葡萄糖;4,6-O-苯亞甲基-D-吡喃葡萄糖;(4AR,7R,8R,8AS)-2-苯基六氫吡喃并[3,2-D][1,3]二氧雜環(huán)己烷基-6,7,8-三醇;(4AR,7R,8R,8AS)-2-苯基六氫吡喃[3,2-D][1,3]二噁英-6,7,8-三醇 |
| 英文名稱 | 4,6-O-Benzylidene-D-glucopyranose |
| 英文同義詞 | 4,6-O-(Phenylmethylene)-D-glucopyranose;4,6-O-Benzylidene-glucopyranos;4,6-O-Benzylidene-glucopyranose;4,4-O-Benzylidene-D-glucopyranose;(4AR,7R,8R,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxine-6,7,8-triol;(4aR,7R,8R,8aS)-2-phenyl-hexahydro-2H-pyrano[3,2-d][1,3]dioxine-6,7,8-triol |
| CAS號 | 97232-16-1 |
| 分子式 | C13H16O6 |
| 分子量 | 268.26 |
| EINECS號 | 824-286-9 |
| 相關(guān)類別 | 醫(yī)藥中間體;Aromatics Compounds;Aromatics;Carbohydrates & Derivatives |
| Mol文件 | 97232-16-1.mol |
| 結(jié)構(gòu)式 | ![]() |
4,6-O-芐叉-D-葡萄糖 性質(zhì)
| 沸點(diǎn) | 483.4±45.0 °C(Predicted) |
|---|---|
| 密度 | 1.436±0.06 g/cm3(Predicted) |
| 儲存條件 | Storage temp. 2-8°C |
| 酸度系數(shù)(pKa) | 11.96±0.70(Predicted) |
| 外觀 | 白色至灰白色固體 |
2280-44-6
1125-88-8
3006-41-5
以(3R,4S,5S,6R)-6-(羥甲基)四氫-2H-吡喃-2,3,4,5-四醇(D-葡萄糖,1.00g,5.55mmol)和苯甲醛二甲縮醛(1.24mL,8.33mmol)為原料,在DMF(11mL)中制備4,6-O-芐烯-D-半乳糖的一般步驟如下:首先將D-葡萄糖在DMF中的懸浮液加熱至60℃直至固體完全溶解。隨后加入苯甲醛二甲基縮醛和對甲苯磺酸一水合物(10mg)。將反應(yīng)混合物在60℃下持續(xù)攪拌6小時(shí),期間每小時(shí)減壓10分鐘以除去生成的MeOH。反應(yīng)完成后,將混合物在真空下濃縮。殘余物通過硅膠柱色譜法(洗脫劑:甲醇/乙酸乙酯,1:10,v/v)進(jìn)行純化,得到目標(biāo)產(chǎn)物吡喃葡萄糖2(799.5mg,2.98mmol,產(chǎn)率53.7%),為白色固體。產(chǎn)物表征數(shù)據(jù)如下:[α]20D +12.9(c 0.20,MeOH);1H-NMR(400MHz,CD3OD)δ 7.46-7.42(m,2H),7.38-7.35(m,3H),6.31(d,J=4.1Hz,0.5H),5.79(d,J=7.8Hz,0.5H),5.60(t,J=9.9Hz,0.5H),5.52(s,0.5H),5.51(s,0.5H),5.37(t,J=9.2Hz,0.5H),5.17-5.10(m,1H),4.39(dd,J=10.3,4.6Hz,0.5H),4.32(dd,J=10.5,5.0Hz,0.5H),4.08-4.00(m,0.5H),3.80-3.63(m,2.5H),2.19(s,1.5H),2.11(s,1.5H),2.08(s,1.5H),2.06(s,1.5H),2.05(s,1.5H),2.04(s,1.5H);13C-NMR(100MHz,CD3OD)δ 139.2, 139.1, 129.9, 129.0, 127.5, 103.0, 102.9, 99.0, 94.7, 83.1, 82.4, 77.2, 74.7, 74.4, 71.8, 70.3, 69.8, 67.7, 63.5;HRMS(ESI)m/z計(jì)算值C13H16O6Na [M+Na]+ 291.0845,實(shí)測值291.0842。
參考文獻(xiàn):
[1] Carbohydrate Research, 2005, vol. 340, # 18, p. 2812 - 2815
[2] Chemical and Pharmaceutical Bulletin, 2001, vol. 49, # 11, p. 1503 - 1505
[3] Journal of Organic Chemistry, 1998, vol. 63, # 23, p. 8491 - 8509
[4] Australian Journal of Chemistry, 1988, vol. 41, # 1, p. 91 - 102
[5] Tetrahedron Letters, 1998, vol. 39, # 16, p. 2299 - 2302
