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131822-46-3

2-CHLORO-3'-METHYLBENZOPHENONE synthesis

4synthesis methods
-

Yield:-

Reaction Conditions:

with erbium(III) triflate in neat (no solvent) at 180; for 0.333333 h;Microwave irradiation;Overall yield = 85 %;Friedel-Crafts Acylation;

Steps:

General procedure

General procedure: mixture of Er(OTf)3 (0.0614 g, 0.1 mmol), anisole(0.5407 g, 5 mmol) and benzoic acid (0.1221 g, 1 mmol) was heated undermicrowave irradiation at 220 C for 30 min in a CEM Discover apparatus. Afterbeing cooled, the mixture was extracted with CH2Cl2 (3 15 mL). The organiclayer was decanted, washed with H2O (10 mL), aqueous NaHCO3 (2 20 mL),and brine (10 mL), and dried over MgSO4. The solvent was removed on a rotaryevaporator. The crude product was purified by flash chromatography (nhexane,then 10% EtOAc in n-hexane) to give 4-methoxybenzophenone(0.153 g, 72% yield). The purity and identity of the product were confirmedby GC-FID, and from GC-MS spectra which were compared with the spectra inthe NIST library, and by 1H and 13C NMR spectroscopy.

References:

Tran, Phuong Hoang;Hansen, Poul Erik;Nguyen, Hai Truong;Le, Thach Ngoc [Tetrahedron Letters,2015,vol. 56,# 4,p. 612 - 618]

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