Benzaldehyde → HCID 66843788, compound
Reaction equation
[CH2:1]([OH:10])[C@@H:2]([C@H:4]([C@@H:6]([CH2:8][OH:9])[OH:7])[OH:5])[OH:3].[CH:11](=O)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.CO.OS(O)(=O)=O>O>[CH:11](=[C:1]([OH:10])[C@@H:2]([C@H:4]([C@@H:6]([CH2:8][OH:9])[OH:7])[OH:5])[OH:3])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
90 Parts by weight of xylitol (75 wt% aqueous solution), 42 parts by weight of benzaldehyde, 60 parts by weight of methanol, 6 parts by weight of conc. H2SO4 and 6 parts by weight of water were reacted with refluxing for two hours. After cooling, the solidified product was ground and washed with water and, then, neutralized with 10 wt% sodium hydroxide aqueous solution followed by washing with water and drying to obtain benzylidenexylitol.
Workup
- temperaturewith refluxing for two hours
- temperatureAfter cooling
- washwashed with water
- washby washing with water
- customdrying
Sources & evidence
- ORD record
- ord-2d476266f99044398848cda76f9c8b9a
- Source dataset
- uspto-grants-1980_01
- Patent number
- US04181527
Reaction notes
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