Salicylamide → HCID 86588640, compound
Reaction equation
[B:1]([OH:4])([OH:3])[OH:2].[OH:5][CH2:6][C@@H:7]([C@H:9]([C@@H:11]([C@@H:13]([CH2:15][OH:16])[OH:14])[OH:12])[OH:10])[OH:8].[C:17]([NH2:26])(=[O:25])[C:18]1[C:19](=[CH:21][CH:22]=[CH:23][CH:24]=1)[OH:20]>C1(C)C=CC=CC=1>[C:17]([NH2:26])(=[O:25])[C:18]1[C:19](=[CH:21][CH:22]=[CH:23][CH:24]=1)[OH:20].[B:1]([OH:4])([OH:3])[OH:2].[OH:16][CH2:15][C@@H:13]([C@H:11]([C@@H:9]([C@@H:7]([CH2:6][OH:5])[OH:8])[OH:10])[OH:12])[OH:14]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Salicylamide/sorbitol borate was prepared as follows. Boric acid (10.3 grams), sorbitol (30.4 grams), and salicylamide (22.9 grams) were added to a 250 milliliter flask. One hundred fifty milliliters of toluene was then added. The reaction was allowed to proceed overnight at 110° C., and the byproduct water (˜9 grams) was continuously removed from the reaction by azeotropic distillation. The final solution was evaporated to remove toluene under vacuum, and a yellowish resinous product (˜55 grams) of salicylamide/sorbitol borate was obtained.
Workup
- customSalicylamide/sorbitol borate was prepared
- customthe byproduct water (˜9 grams) was continuously removed from the reaction by azeotropic distillation
- customThe final solution was evaporated
- customto remove toluene under vacuum
Sources & evidence
- ORD record
- ord-8662594b1535487886a1ff3b99e0f72c
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06682591B2
Reaction notes
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