Isopropyl 2-naphthyl ether

Maltol Isobutyrate 2-Methoxy 3-(or 5- or 6-) Isopropyl Pyrazine 5H-5-Methyl-6,7 -dihydrocyclopenta[b]pyrazine 5-Methyl Furfural Methyl Furoate Methyl Hexanoate Methyl Isovalerate 5-Methyl 2-Phenyl 2-Hexenal Methyl Thiobutyrate Methyl Valerate P-Naphthyl Ethyl Ether Phenyl Ethyl Cinnamate Phenyl Ethyl Propionate Propyl Formate Propyl Mercaptan Salicylaldehyde 8-T etradecalactone 2-Tridecanone... 

Alcohols. Methanol and ethanol have long been important alkylating agents, especially for nitrogen bonding. In practically every case, a catalyst is necessary to cause the alkylation to proceed smoothlyvand in many instances, this is a mineral acid. Alcohols are used in the manufacture of ethers, such as ordinary ethyl ether, isopropyl ether, Carbitol, Cellosolve, and naphthyl methyl ether. It should be noted that, although naphthols react with alcohol in the presence of a mineral acid, the aryl alkyl ethers cannot be formed by this reaction in the case of phenols. 

The use of another acyl donor such as isopropyl methoxyacetate has allowed the resolution of 1-phenylethlamine-substituted derivatives under free solvent conditions in the presence of CAL-B [190], this also being effective for aliphatic amines containing long side chains, and naphthyl and pyridine derivatives using the same lipase and diethyl ether (EtjO) as solvent (Figure 9.24) [191]. 

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