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D-(-)-Fructose → Hydrochloric Acid

HRID 239232
ノート
印刷プレビュー

反応式

HRID 239232 の反応式
[O:1]=[CH:2][C@@H:3]([C@H:5]([C@@H:7]([C@@H:9]([CH2:11][OH:12])[OH:10])[OH:8])[OH:6])[OH:4].[OH:13]CC([C@H:17]([C@@H:19]([C@@H:21]([CH2:23][OH:24])O)O)O)=O.[Cl-:25].C([N+]1C=CN(C)C=1)C.[Na+:34].[Br-].B([O-])([O-])[O-]>[Cr].Cl.CN(C)C=O.CC(N(C)C)=O.O>[O:1]=[CH:2][C@@H:3]([C@H:5]([C@@H:7]([C@@H:9]([CH2:11][OH:12])[OH:10])[OH:8])[OH:6])[OH:4].[ClH:25].[OH2:13].[Na+:34].[Cl-:25].[CH2:19]1[CH2:17][O:24][CH2:23][CH2:21]1
参加物実験手順後処理出典と根拠反応ノート

参加物

13

反応物 5

HCID 5984D-(-)-Fructose4 回HCID 26574BorateHCID 107526(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal7 回HCID 253881Sodium BromideHCID 178462722HCID 178462722、化合物

生成物 3

HCID 313Hydrochloric Acid
HCID 107526
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal
HCID 131731185water NaCl THF

試薬・触媒・溶媒 5

HCID 313Hydrochloric Acid触媒HCID 23976Chromium触媒HCID 962Water溶媒HCID 6228Dimethylformamide溶媒HCID 31374Dimethylacetamide溶媒

実験手順

Recent studies have been published on developing new processing strategies focused on isomerizing glucose to fructose with a subsequent acid-catalyzed dehydration of fructose to HMF. Lewis acid catalysts in ionic liquids have been shown to be the most promising systems for the conversion of glucose to HMF.1e Zhao, et al. first reported HMF yields of 68-70% in a system consisting of 1-ethyl-3-methyl-imidazolium chloride and a CrCl2 catalyst.1b It is believed that the high activity and selectivity observed for the production of HMF in ionic liquids with chromium catalysts are caused by the stabilization of the transition state for ring opening of glucose by the Lewis acidic Cr center during glucose isomerization.7 Other studies have been carried out on this same reaction using different ionic liquids or Lewis acid catalysts.8 However, the reactions require ionic liquids, which are expensive and subject to deactivation by small amounts of water formed during dehydration reactions.9 Binder, et al. reported that a mixture consisting of dimethylacetamide (DMA), NaBr, and a Lewis acid, CrCl2, could reach HMF yields of 81%, being as effective as ionic liquid systems.1c Huang, et al. reported an HMF yield of 63% from glucose by a two-step process consisting of the isomerization of glucose to fructose in the presence of glucose isomerase and borate ions, followed by the acid catalyzed dehydration of fructose to HMF using HCl as a catalyst in a biphasic system.10 Takagaki, et al. reported HMF yields of 42% at a 73% conversion by a similar two step process by combining a solid acid catalyst, Amberlyst-15, and a solid base catalyst, Mg—Al hydrotalcite, in N,N-dimethylformamide.11 Nikolla, et al. reported HMF yields of 57% at 79% conversion of glucose using a Lewis acidic Sn-Beta zeolite and HCl in a water/NaCl/THF biphasic reaction system.12

後処理

  1. customHMF yields of 68-70% in a system
  2. customhave been carried out on this same reaction
  3. customformed during dehydration reactions.9 Binder, et al.
  4. customyields of 81%
  5. customyields of 42% at a 73% conversion by a similar two step process

出典と根拠

ORDレコード
ord-2b34dc07561a4c85b00af92813cc3f50
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08642791B2

反応ノート

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