Список литературы по синтезу Фенилэтанола 2
1: Reduction of phenylacetaldehyde with sodium amalgam in aqueous alcohol (Radziszewski, Ber., 9 (1876) 373.)
2: Reduction of phenylacetaldehyde by hydrogen with nickel or palladium catalysts (Skita and Rojahn, Ber., 33 (1900) 1723)
3: Phenyl acetic acid reduction by Bouveault-Blanc reduction (sodium in absolute alcohol). (Bouveault and Blanc, compt Rend, 137 (1903) 61.)
4: Phenyl acetic acid reduction by sodium aluminum hydride in THF. (Pitha, Hermanek and Vit (Collection Czech Chem. Commun.,25 (1960) 736; C. A., 54 (1960) 13055.
5: alkaline borohydride reduction of esters (Paul and Joseph, Bull. Soc. Chim. France, (1952) 550
6:Ethyl phenyl acetate in liquid ammonia using sodamide (Chabley, Compt. Rend. 156 (1913) 1022.
7: Electrolytic reduction of phenylacetic acid in 75% sulfuric acid with a lead cathode gives phely ethyl phenylacetate which can be saponified to give phenylethyl alcohol. (Marie, Marquis and Birkenstock, (Bull. Soc. Chim. France, [4], 24 (1919) 513.
8: Styrene plus Hydrogen chloride to give phenyl ethyl chloride, which on hydrolysis with weak aqueous alkalis gives phenylethyl alcohol. (Britton, Coleman and Hadler, US patent 2,185,141 Dec. 26, 1939 )
1: Reduction of phenylacetaldehyde with sodium amalgam in aqueous alcohol (Radziszewski, Ber., 9 (1876) 373.)
2: Reduction of phenylacetaldehyde by hydrogen with nickel or palladium catalysts (Skita and Rojahn, Ber., 33 (1900) 1723)
3: Phenyl acetic acid reduction by Bouveault-Blanc reduction (sodium in absolute alcohol). (Bouveault and Blanc, compt Rend, 137 (1903) 61.)
4: Phenyl acetic acid reduction by sodium aluminum hydride in THF. (Pitha, Hermanek and Vit (Collection Czech Chem. Commun.,25 (1960) 736; C. A., 54 (1960) 13055.
5: alkaline borohydride reduction of esters (Paul and Joseph, Bull. Soc. Chim. France, (1952) 550
6:Ethyl phenyl acetate in liquid ammonia using sodamide (Chabley, Compt. Rend. 156 (1913) 1022.
7: Electrolytic reduction of phenylacetic acid in 75% sulfuric acid with a lead cathode gives phely ethyl phenylacetate which can be saponified to give phenylethyl alcohol. (Marie, Marquis and Birkenstock, (Bull. Soc. Chim. France, [4], 24 (1919) 513.
8: Styrene plus Hydrogen chloride to give phenyl ethyl chloride, which on hydrolysis with weak aqueous alkalis gives phenylethyl alcohol. (Britton, Coleman and Hadler, US patent 2,185,141 Dec. 26, 1939 )
