Sodium ethoxide → Ethyl 7-(2-chloroethoxy)-6-methoxy-3-nitro-2-naphthoate

反応式

[N+:1]([CH2:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])([O-:3])=[O:2].[O-]CC.[Na+].[Cl:15][CH2:16][CH2:17][O:18][C:19]1[CH:20]=[C:21]([CH:29]=O)[C:22](=[CH:25][C:26]=1[O:27][CH3:28])[CH:23]=O>C(O)C>[Cl:15][CH2:16][CH2:17][O:18][C:19]1[CH:20]=[C:21]2[C:22]([CH:23]=[C:4]([N+:1]([O-:3])=[O:2])[C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:29]2)=[CH:25][C:26]=1[O:27][CH3:28]

参加物

実験手順

To a solution of 2.43 g of ethyl 3-nitropropionate in 15 ml of absolute ethanol cooled using an ice bath, is added 20 mL of 1 N sodium ethoxide in ethanol dropwise over 10 minutes keeping the temperature at 0–5° C. A slurry of 4-(2-chloroethoxy)-5-methoxyphthalaldehyde in 5 mL of ethanol is added. The ice bath is removed and the reaction allowed to warm to room temperature and stirred for 16 hours. The reaction is transferred to a beaker with 300 mL of water and neutralized with acetic acid to pH 4. The solid is collected and washed first with water, then with 40 mL of cold ethanol. The solid is dried to provide 2.48 g (70%) of ethyl 7-(2-chloroethoxy)-6-methoxy-3-nitro-2-naphthoate and ethyl 6-(2-chloroethoxy)-7-methoxy-3-nitro-2-naphthoate (1:1 mixture) as a yellow solid, m.p. 119–29° C. dec.