m-Chloroperbenzoic acid → HCID 59717846, compound
Reaction equation
ClC1C=CC=[C:4]([C:8]([O:10]O)=[O:9])C=1.[CH2:12]([O:14][C:15](=[O:35])[NH:16][CH2:17][CH2:18][C:19]1[CH:24]=[CH:23][C:22]([O:25][C:26]2[CH:31]=[CH:30][C:29](C(=O)C)=[CH:28][CH:27]=2)=[CH:21][CH:20]=1)[CH3:13]>C(Cl)(Cl)Cl>[CH2:12]([O:14][C:15]([NH:16][CH2:17][CH2:18][C:19]1[CH:20]=[CH:21][C:22]([O:25][C:26]2[CH:27]=[CH:28][C:29]([O:10][C:8](=[O:9])[CH3:4])=[CH:30][CH:31]=2)=[CH:23][CH:24]=1)=[O:35])[CH3:13]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Metachloroperbenzoic Acid (1.2 g, 4.1 mmol) was added to a solution of {2-[4-(4-acetyl-phenoxy)-phenyl]-ethyl}-carbamic acid ethyl ester (1.0 g, 3.1 mmol) in chloroform (75 mL). Stirred at room temperature for 72 hours, quenched with saturated aqueous Na2S2O3, then extracted with dichloromethane (3×75 mL). The combined dichloromethane extracts were dried over sodium chloride/magnesium sulfate, filtered, and concentrated on a rotary evaporator to yield the crude product (2 g). The crude product was purified by flash column chromatography on silica gel eluting with ethyl acetate and hexanes to yield Acetic acid 4-[4-(2-ethoxycarbonylamino-ethyl)-phenoxy]-phenyl ester (430 mg). 1H NMR (CDCl3, 300.00 MHz): 7.19-6.92 (m, 8H), 4.98 (s, 1H), 4.17-4.07 (m, 2H), 3.42 (q, 2H, J=6.6 Hz), 2.79 (t, 2H, J=7.2 Hz), 2.29 (s, 3H), 1.30-1.20 (m, 3H), 1.30-1.20 (m, 3H), 1.30-1.20 (m, 3H).
Workup
- customquenched with saturated aqueous Na2S2O3
- extractionextracted with dichloromethane (3×75 mL)
- dry with materialThe combined dichloromethane extracts were dried over sodium chloride/magnesium sulfate
- filtrationfiltered
- concentrationconcentrated on a rotary evaporator
- customto yield the crude product (2 g)
- customThe crude product was purified by flash column chromatography on silica gel eluting with ethyl acetate and hexanes
Sources & evidence
- ORD record
- ord-9c1e0cb0de914c649dde25400f6949e6
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08338611B2
Reaction notes
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