反応式
[C:1]([CH2:9][C:10]([O:12]CC)=O)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:15][O:16][C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([NH2:23])[CH:18]=1.Cl.O1CCOCC1.C(O)[C@H](O)[C@H]1OC(=O)C(O)=C1O>C1(C)C=CC=CC=1>[OH:12][C:10]1[C:20]2[C:19](=[CH:18][C:17]([O:16][CH3:15])=[CH:22][CH:21]=2)[N:23]=[C:1]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:9]=1参加物
反応条件
- 温度
- 280 °C
実験手順
A solution of ethyl benzoylacetate (b) (100.0 g, 0.52 mol), m-anisidine (a) (128.1 g, 1.04 mol) and 4 N HCl/dioxane (5.2 mL) in toluene (1.0 L) was refluxed for 6.25 h in a Dean-Stark apparatus. The cooled toluene solution was successively washed with aqueous 10% HCl (2×300 mL), 1 N NaOH (2×300 mL), H2O (300 mL) and brine (150 mL). The toluene phase was dried (MgSO4), filtered and concentrated under reduced pressure to give a 1.2:1.0 mixture of ester c and amide d (144.6 g, 45%/38% crude yield) as a dark brown oil. The crude oil was heated to 280° C. for 80 min while distilling generated EtOH. The cooled dark solid obtained was triturated with CH2Cl2 (200 mL). The suspension was filtered and the resulting solid washed with CH2Cl2 to give e (22.6 g, 17% from a) as a beige solid: 1H NMR (DMSO-d6) δ 8.00 (d, J=9.0 Hz, 1H), 7.81-7.82 (m, 2H), 7.57-7.59 (m, 3H), 7.20 (d, J=2.2 Hz, 1H), 6.94 (dd, J=9.0, 2.2 Hz, 1H), 6.26 (s, 1H), 3.87 (s, 3H).
後処理
- washThe cooled toluene solution was successively washed with aqueous 10% HCl (2×300 mL), 1 N NaOH (2×300 mL), H2O (300 mL) and brine (150 mL)
- dry with materialThe toluene phase was dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customto give
- distillationwhile distilling
- customThe cooled dark solid obtained
- customwas triturated with CH2Cl2 (200 mL)
- filtrationThe suspension was filtered
- washthe resulting solid washed with CH2Cl2
- customto give e (22.6 g, 17% from a) as a beige solid
出典と根拠
- ORDレコード
- ord-14a51161b171474ab725977e128c4cea
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- USRE040525E1
関連ノート
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