Chloroform → HCID 13650573, compound
Reaction equation
[CH2:1]([C:4]1[C:17]([OH:18])=[C:16]([Cl:19])[C:15]2[O:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:20])[C:6]=2[CH:5]=1)[CH:2]=C.ClC1C=CC=C(C(OO)=O)C=1.C(Cl)(Cl)Cl.[C:36](=[O:39])([O-])[O-:37].[K+].[K+]>O>[Cl:19][C:16]1[C:15]2[O:14][C:13]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[C:7](=[O:20])[C:6]=2[CH:5]=[C:4]2[CH2:1][CH:2]([C:36]([OH:37])=[O:39])[O:18][C:17]=12Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 2-allyl-4-chloro-3-hydroxy-9-oxo-9H-xanthene (2.0 g), m-chloroperbenzoic acid (3.6 g) and chloroform (100 ml) was stirred at room temperature for 5 hours and thereafter left to stand overnight. To the mixture, potassium carbonate (8 g) and water (200 ml) were added and the resulting mixture was extracted with chloroform. The chloroform layer was dried and the solvent was distilled off. The residue was dissolved in acetone (400 ml) and to the stirred solution, a mixture of chromium trioxide (1.7 g), water (10 ml) and concentrated sulfuric acid (3 g) was added dropwise at room temperature. After standing overnight, the mixture was filtered and the filtrate was evaporated to dryness under vacuum. After addition of water, the solid crystal was recovered by filtration, washed with water and dried. Recrystallization from ethanol gave 0.9 g of 11-chloro-2,3-dihydro-5-oxo-5H-furo[3,2-b]xanthene-2-carboxylic acid. m.p. 290°-293° C. This compound exhibited a mass spectrum having a molecular ion peak at m/e 316.
Workup
- waitleft
- waitto stand overnight
- extractionthe resulting mixture was extracted with chloroform
- dry with materialThe chloroform layer was dried
- distillationthe solvent was distilled off
- dissolutionThe residue was dissolved in acetone (400 ml) and to the stirred solution
- additiona mixture of chromium trioxide (1.7 g), water (10 ml) and concentrated sulfuric acid (3 g)
- additionwas added dropwise at room temperature
- waitAfter standing overnight
- filtrationthe mixture was filtered
- customthe filtrate was evaporated to dryness under vacuum
- additionAfter addition of water
- filtrationthe solid crystal was recovered by filtration
- washwashed with water
- customdried
- customRecrystallization from ethanol
Sources & evidence
- ORD record
- ord-4fd353255a2f4633a798d8191c38be6f
- Source dataset
- uspto-grants-1987_04
- Patent number
- US04661607
Reaction notes
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