![](/CAS/GIF/4504-87-4.gif)
Dibenz[b,e]oxepin-11(6H)-one synthesis
- Product Name:Dibenz[b,e]oxepin-11(6H)-one
- CAS Number:4504-87-4
- Molecular formula:C14H10O2
- Molecular Weight:210.23
![2-(Phenoxymethyl)benzoic acid](/CAS/GIF/724-98-1.gif)
724-98-1
67 suppliers
$25.89/1g
![Dibenz[b,e]oxepin-11(6H)-one](/CAS/GIF/4504-87-4.gif)
4504-87-4
164 suppliers
$5.00/250mg
Yield: 98%
Reaction Conditions:
with trifluoromethylsulfonic anhydride;boron trifluoride diethyl etherate in dichloromethane at 40; for 2 h;
Steps:
237.1 Step 1: dibenzo[b,e]oxepin-11(6H)-one (482)
The 2-(phenoxymethyl)benzoic acid (22.18 g, 97 mmol) was dissolved in DCM (200 mL) and trifluoroacetic anhydride (20.59 mL, 146 mmol) was added, followed by a catalytic amount of borontrifluoride etherate (2.22 mL, 17.5 mmol). The reaction mixture was heated at 40° C. for 2 hours. The solution was then washed with water, sodium bicarbonate (saturated solution) and water. The organic phases was dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified on silica gel (10-20% ethyl acetate in hexanes) to afford title compound 482 (19.937 g, 98%) as a light pink solid. MS (m/z): 211.1 (M+H).
References:
Forum Pharmaceuticals, Inc.;Rogers, Kathryn;Patzke, Holger US2017/749, 2017, A1 Location in patent:Paragraph 0719
![Phthalide](/CAS/GIF/87-41-2.gif)
87-41-2
458 suppliers
$6.00/10g
![Dibenz[b,e]oxepin-11(6H)-one](/CAS/GIF/4504-87-4.gif)
4504-87-4
164 suppliers
$5.00/250mg
![2-(PHENOXYMETHYL)BENZOYL CHLORIDE 97](/CAS/GIF/21733-94-8.gif)
21733-94-8
6 suppliers
inquiry
![Dibenz[b,e]oxepin-11(6H)-one](/CAS/GIF/4504-87-4.gif)
4504-87-4
164 suppliers
$5.00/250mg
![ETHYL 2-(BROMOMETHYL)BENZOATE](/CAS/GIF/7115-91-5.gif)
7115-91-5
90 suppliers
$29.00/100mg
![Dibenz[b,e]oxepin-11(6H)-one](/CAS/GIF/4504-87-4.gif)
4504-87-4
164 suppliers
$5.00/250mg
![Phenol](/CAS/20180808/GIF/108-95-2.gif)
108-95-2
724 suppliers
$14.00/25g
![Dibenz[b,e]oxepin-11(6H)-one](/CAS/GIF/4504-87-4.gif)
4504-87-4
164 suppliers
$5.00/250mg