Reaction equation
CC([O:4][CH2:5][C@H:6]1[O:11][C@H:10]([O:12][C@:13]2([CH2:22][Cl:23])[O:17][C@H:16]([CH2:18][Cl:19])[C@@H:15]([OH:20])[C@@H:14]2[OH:21])[C@H:9]([OH:24])[C@@H:8]([OH:25])[C@H:7]1[Cl:26])=O.C[O-].[Na+]>CO>[CH2:5]([OH:4])[C@@H:6]1[O:11][C@H:10]([O:12][C@:13]2([CH2:22][Cl:23])[O:17][C@H:16]([CH2:18][Cl:19])[C@@H:15]([OH:20])[C@@H:14]2[OH:21])[C@@H:9]([OH:24])[C@@H:8]([OH:25])[C@H:7]1[Cl:26]Participants
4
Procedure
A mixture of 20 g of dry sucralose-6-acetate obtained from Example 5 and 70 ml of methanol was heated to from 40° C. to 50° C. When the reacting mixture became a clear solution, a small quantity of a 30% sodium methylate solution was added. After the mixture was stirred for 2 hours, methanol was removed under reduced pressure. The resultant mixture was diluted to a 30% mixture by adding a certain quantity of water, which was decolored and then filtered. The filtrate thus obtained was concentrated to a 65% solution, which was cooled to form crystallized sucralose. The obtained crystal was filtered and dried to give sucralose with a yield of over 95% and purity of over 98.0%.
Workup
- temperaturewas heated to from 40° C. to 50° C
- custommethanol was removed under reduced pressure
- additionThe resultant mixture was diluted to a 30% mixture
- additionby adding a certain quantity of water, which
- filtrationfiltered
- customThe filtrate thus obtained
- concentrationwas concentrated to a 65% solution, which
- temperaturewas cooled
- customto form
- customcrystallized sucralose
- filtrationThe obtained crystal was filtered
- customdried
Sources & evidence
- ORD record
- ord-89542098a95b4599bac600c077c6b4da
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07626016B2
Linked notes
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