1-(chloromethyl)-2-(trifluoromethoxy)benzene

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of intermediate 25 (200 mg, 0.786 mmol) and 2-trifluoromethoxybenzyl chloride (0.331 mg, 1.57 mmol) in abs. EtOH (2 mL) is heated at 95° C. for 24 h. The reaction mixture is cooled to RT, evaporated to dryness, and the residue suspended in Et2O. The insoluble material is filtered to give 202 mg of the product 215. 1H NMR (DMSO-d6) δ 11.32 (s, 2 H), 7.85 (d, 1 H), 7.70-7.40 (m, 3 H), 7.20-6.70 (m, 10 H), 5.80 (s, 2 H), 4.85 (s, 2 H); MS: m/z 429 (M++1). evaporated to dryness The insoluble material is filtered

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of intermediate 25 (200 mg, 0.786 mmol) and 2-trifluoromethoxybenzyl chloride (0.331 mg, 1.57 mmol) in abs. EtOH (2 mL) is heated at 95° C. for 24 h. The reaction mixture is cooled to RT, evaporated to dryness, and the residue suspended in Et2O. The insoluble material is filtered to give 202 mg of the product 215. 1H NMR (DMSO-d6) δ 11.32 (s, 2 H), 7.85 (d, 1 H), 7.70-7.40 (m, 3 H), 7.20-6.70 (m, 10 H), 5.80 (s, 2 H), 4.85 (s, 2 H); MS: m/z 429 (M++1). evaporated to dryness The insoluble material is filtered

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of intermediate 25 (200 mg, 0.786 mmol) and 2-trifluoromethoxybenzyl chloride (0.331 mg, 1.57 mmol) in abs. EtOH (2 mL) is heated at 95° C. for 24 h. The reaction mixture is cooled to RT, evaporated to dryness, and the residue suspended in Et2O. The insoluble material is filtered to give 202 mg of the product 215. 1H NMR (DMSO-d6) δ 11.32 (s, 2H), 7.85 (d, 1H), 7.70-7.40 (m, 3H), 7.20-6.70 (m, 10H), 5.80 (s, 2H), 4.85 (s, 2H); MS: m/z 429 (M++1). evaporated to dryness The insoluble material is filtered

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of intermediate 25 (200 mg, 0.786 mmol) and 2-trifluoromethoxybenzyl chloride (0.331 mg, 1.57 mmol) in abs. EtOH (2 mL) is heated at 95° C. for 24 h. The reaction mixture is cooled to RT, evaporated to dryness, and the residue suspended in Et2O. The insoluble material is filtered to give 202 mg of the product 215. 1H NMR (DMSO-d6) δ 11.32 (s, 2 H), 7.85 (d, 1 H), 7.70-7.40 (m, 3 H), 7.20-6.70 (m, 10 H), 5.80 (s, 2 H), 4.85 (s, 2 H); MS: m/z 429 (M++1). evaporated to dryness The insoluble material is filtered