alpha-D-glucopyranosyl-(1->6)-D-mannose → Isomaltitol

HRID 341902

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HRID 341902 반응식
[C@H:1]1([O:12][CH2:13][C@@H:14]([OH:23])[C@@H:15]([OH:22])[C@H:16]([OH:21])[C@H:17]([OH:20])[CH:18]=[O:19])[O:9][C@H:8]([CH2:10][OH:11])[C@@H:6]([OH:7])[C@H:4]([OH:5])[C@H:2]1[OH:3]>C(O)[C@H]1O[C@H](OC[C@H]2OC(O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O>[CH2:10]([OH:11])[C@H:8]1[O:9][C@H:1]([O:12][CH2:13][C@@H:14]([OH:23])[C@@H:15]([OH:22])[C@H:16]([OH:21])[C@H:17]([OH:20])[CH2:18][OH:19])[C@H:2]([OH:3])[C@@H:4]([OH:5])[C@@H:6]1[OH:7].[CH2:10]([OH:11])[C@H:8]1[O:9][C@H:1]([O:12][CH2:13][C@@H:14]([OH:23])[C@@H:15]([OH:22])[C@H:16]([OH:21])[C@@H:17]([OH:20])[CH2:18][OH:19])[C@H:2]([OH:3])[C@@H:4]([OH:5])[C@@H:6]1[OH:7].[CH2:10]([OH:11])[C@H:8]1[O:9][C@H:1]([O:12][CH2:13][C@@H:14]([OH:23])[C@@H:15]([OH:22])[C@H:16]([OH:21])[C@@H:17]([OH:20])[CH2:18][OH:19])[C@H:2]([OH:3])[C@@H:4]([OH:5])[C@@H:6]1[OH:7]

참가 물질

4

실험 절차

In the process according to the invention, the depletion of the epimerized mixture in isomaltose is, on the contrary, carried out in such a manner as to obtain a fraction containing a roughly equimolecular proportion of isomaltose and α-D-glucopyranosyl-(1→6)-D-mannose, the other fraction being constituted by very pure isomaltose. By roughly equimolecular is meant from 40 to 60% and more preferably from 45 to 55% of one of the two compounds relative to the total mass of the two compounds. This way of proceeding has the advantage of directly obtaining a mixture which after hydrogenation will provide the two components of palatinitol, namely isomaltitol and GPM in roughly equimolecular proportions, without having to resort to remixing pure fractions.

후처리

  1. customto obtain a fraction
  2. customof directly obtaining a mixture which after hydrogenation

출처 및 근거

ORD 기록
ord-19b8ce0752ca4c2b96638b594f446aff
출처 데이터셋
uspto-grants-1999_01
특허 번호
US05856469

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