Benzoin → HCID 131710645, compound
Reaction equation
[C:1]1([C:7]([CH:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[OH:10])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:17][O:18][CH:19]1[CH2:24][CH2:23][CH:22]=[CH:21][O:20]1>C1C=CC=CC=1>[CH3:17][O:18][C:19]1([O:8][CH:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[C:9](=[O:10])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:24][CH2:23][CH2:22][CH2:21][O:20]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
85 parts of benzoin are reacted with 68.4 parts (50% molar excess) of 2-methoxy-2,3-dihydro-4H-pyran in 120 parts by volume of benzene, analogously to Example 1. The resulting benzoin 2-methoxy-tetrahydropyranyl ether, obtained in a yield of 87.4% of theory, boils at 195° to 200° C/0.3 mm Hg and has the following structure: ##STR7## NMR spectrum (in CDCl3): δ = 1.0 -2.4 (multiplet, 6 protons)
Sources & evidence
- ORD record
- ord-d843bf137d3348c1b117b077a1b547e7
- Source dataset
- uspto-grants-1977_02
- Patent number
- US04007209
Reaction notes
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