Sulfuric Acid → 4-Hydroxy-7-(2-hydroxy-3-phenoxypropoxy) coumarin
Reaction equation
[OH:1][CH:2]([CH2:17][O:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH2:3][O:4][C:5]1[CH:14]=[C:13]2[C:8]([C:9](=N)[CH2:10][C:11](=[O:15])[O:12]2)=[CH:7][CH:6]=1.S(=O)(=O)(O)[OH:26]>>[OH:26][C:9]1[C:8]2[C:13](=[CH:14][C:5]([O:4][CH2:3][CH:2]([OH:1])[CH2:17][O:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)=[CH:6][CH:7]=2)[O:12][C:11](=[O:15])[CH:10]=1Participants
Procedure
A solution of 3,4-dihydro-7-(2-hydroxy-3-phenoxypropoxy)-4-iminocoumarin (6.5 g; 0.02 mole) in 50% w/v sulphuric acid (80 g) was stirred at 100° for 3-6 hours. The initial pale red solution precipitated a yellow solid which after cooling and dilution with water was separated by decantation. After several decantations with water the oily solid was taken up in hot ethanol, charcoaled, filtered and the filtrate gradually diluted with water. The precipitated oily solid crystallised overnight to give 2.934 of buff solid of m.p. 145°-175°. Recrystallisation from aqueous methanol gave 2.275 g (34%) of material of m.p. 181°-183°, νmax (mull) 3250, 3060, 1705, 1610 cm-1 ; τ(DMSO); 5.85 (5H, m); 4.75 (1H broad exchangeable); 4.50 (1H, sharp exchangeable singlet); 3.19-2.50 (7H, complex m); 2.22 (1H, d, J 9.0 Hz); 1 low field exchangeable singlet. (Found; C, 65.48; H, 5.19; C18H16O6 requires; C, 65.85; H, 4.91%)
Workup
- customThe initial pale red solution precipitated a yellow solid which
- temperatureafter cooling
- customdilution with water was separated by decantation
- filtrationfiltered
- additionthe filtrate gradually diluted with water
- customThe precipitated oily solid crystallised overnight
- customto give 2.934 of buff solid of m.p. 145°-175°
- customRecrystallisation from aqueous methanol
Sources & evidence
- ORD record
- ord-7cdc276739324ee8835f6592635da00e
- Source dataset
- uspto-grants-1980_06
- Patent number
- US04207335
Reaction notes
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