(2R)-2-methoxy-2-phenylethanol

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

Procedure: 72 g of (R)-2-phenyl-2-methoxyacetic acid (prepared according to the method described in J. Chem. Soc., 1962, p. 1519), are reduced with 16.5 g of lithium aluminum hydride in 300 ml of tetrahydrofuran.

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

Procedure: 72 g of (R)-2-phenyl-2-methoxyacetic acid (prepared according to the method described in J. Chem. Soc., 1962, p. 1519), are reduced with 16.5 g of lithium aluminum hydride in 300 ml of tetrahydrofuran.

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

Procedure: 72 g of (R)-2-phenyl-2-methoxyacetic acid (prepared according to the method described in J. Chem. Soc., 1962, p. 1519), are reduced with 16.5 g of lithium aluminum hydride in 300 ml of tetrahydrofuran.

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

Procedure: 72 g of (R)-2-phenyl-2-methoxyacetic acid (prepared according to the method described in J. Chem. Soc., 1962, p. 1519), are reduced with 16.5 g of lithium aluminum hydride in 300 ml of tetrahydrofuran.