Benzbromarone synthesis
- Product Name:Benzbromarone
- CAS Number:3562-84-3
- Molecular formula:C17H12Br2O3
- Molecular Weight:424.08
1477-19-6
145 suppliers
$15.00/100mg
3562-84-3
324 suppliers
$25.00/500mg
Yield:3562-84-3 35%
Reaction Conditions:
with bromine;acetic acid for 0.25 h;Product distribution / selectivity;
Steps:
In a RBF/SB (50 mL), hydroxy-benzofuran (13; 318 mg; 1.19 mmol) was diluted with AA (20 mL) and then Br2 (138 μ) was added. After 15 min, the mixture was quenched with H20 (35 mL) and extracted with EtOAc (3 x 70 mL). The organic phase was washed NaCl aq (2 x 50 mL) and dried (MgS04), filtered, concentrated under reduced pressure, and purified via Si02 chromatography (3:1 ; Hex:EtOAc) to give 7 as a light red solid (176 mg; 0.469 mmol; 35% yield). 1H-NMR (400 MHz) DMSO-d6: 10.2 (bs, 1H; exchangeable in D20), 7.91 (s, 2H), 7.66-7.64 (d, 1H), 7.43-7.41 (d, 1H), 7.36-7.33 (t, 1H), 7.29-7.27 (d, 1H), 2.83-2.77 (q, 2H), 1.28-1.24 (t, 3H); 13C-NMR (100 MHz) DMSO-d6: 187.5, 165.8, 156.1, 153.5, 133.7,132.3, 126.9, 125.2, 124.3, 121.2, 1 15.6, 1 12.2, 1 11.7, 21.84, 12.4. LC/MS-MS: 424.9 -> 278.8 m/z; GS1 and GS2 at 20, DP = 96, CE = 37, CXP = 16, tR = 4.65 min.
References:
J-PHARMA CO., LTD.;WEMPE, Michael, F.;ENDOU, Hitoshi WO2012/48058, 2012, A2 Location in patent:Page/Page column 15
3343-80-4
16 suppliers
inquiry
3562-84-3
324 suppliers
$25.00/500mg
3131-63-3
181 suppliers
$10.00/5g
3562-84-3
324 suppliers
$25.00/500mg
1477-19-6
145 suppliers
$15.00/100mg
68-90-6
49 suppliers
$62.50/5 mg
3562-84-3
324 suppliers
$25.00/500mg
100-07-2
398 suppliers
$23.69/5g
3562-84-3
324 suppliers
$25.00/500mg