Kojic Acid → Chlorokojic acid
Reaction equation
[CH:1]1[C:6](=[O:7])[C:5]([OH:8])=[CH:4][O:3][C:2]=1[CH2:9]O.S(Cl)([Cl:13])=O>C(#N)C>[CH:1]1[C:6](=[O:7])[C:5]([OH:8])=[CH:4][O:3][C:2]=1[CH2:9][Cl:13]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 2-liter 3-neck round bottom flask was equipped with a mechanical stirrer. The flask was charged with kojic acid (0.25 kg, 1.759 mol) and 750 ml acetonitrile at 0° C. The kojic acid was insoluble in acetonitrile and stayed as a suspension. Thionyl chloride (140 ml, 1.919 mol) was added dropwise via a dropping funnel at ice bath temperature. The solid slowly dissolved to give a red clear solution. After 15 minutes, a white solid appeared. After 3 hrs at 0° C., the insoluble solid was filtered. The solid was filtered by suction filtration. The solid was mixed with water (0.5L) and then filtered. The acetonitrile mother liquor was reduced to 15% of the original volume and filtered. The solid was washed with water (200 ml) and then acetonitrile (50 ml). The combined solid was dried to constant weight (269 g, 95.2% yield). M.p. 166-1680° C. [lit value 166-167° C.]. 1H-NMR (DMSO-d6) δ: 4.66 (s, 2H, CH2Cl), 6.57 (s, 1H, CH), 8.12 (s, 1H, CH), 9.3 (br. s, 1H, OH).
Workup
- customA 2-liter 3-neck round bottom flask was equipped with a mechanical stirrer
- dissolutionThe solid slowly dissolved
- customto give a red clear solution
- waitAfter 3 hrs at 0° C.
- filtrationthe insoluble solid was filtered
- filtrationThe solid was filtered by suction filtration
- additionThe solid was mixed with water (0.5L)
- filtrationfiltered
- filtrationfiltered
- washThe solid was washed with water (200 ml)
- customThe combined solid was dried to constant weight (269 g, 95.2% yield)
- customM.p. 166-1680° C. [lit value 166-167° C.]
Sources & evidence
- ORD record
- ord-d0f6795b496a419ebe99cf98ae2614d1
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06472532B1
Reaction notes
Loading…