反応式
[NH2:1][CH2:2][CH2:3][OH:4].[Cl:5][C:6]1[CH:7]=[C:8]([CH:13]=[C:14]([Cl:17])[C:15]=1[OH:16])[C:9](OC)=[O:10].Cl>O>[Cl:5][C:6]1[CH:7]=[C:8]([CH:13]=[C:14]([Cl:17])[C:15]=1[OH:16])[C:9]([NH:1][CH2:2][CH2:3][OH:4])=[O:10]参加物
反応条件
- 温度
- 80 °C
実験手順
A 2 L, 3 necked, round bottom flask was charged with 2-aminoethanol (240 gm; 3.93 moles) and heated to 80° C. Methyl 3,5-dichloro-4-hydroxybenzoate (432 gm; 1.96 moles) was added in portions through a powder funnel. The resulting amber solution was heated to 145° C. and the liberated methanol distilled into a Dean Stark trap. The reaction required about 3.5 hrs. Upon completion, the solution was cooled to 90°-100° C. and dissolved in 1.95 L H2O. The aqueous solution was cooled to 25° C., placed in an ice bath and made slightly acidic with concentrated hydrochloric acid (196 ml; 2.35 moles). The product precipitated and filtration afforded a white solid. After drying at 50° C. in a vacuum oven, the product darkened slightly. The crude material (384.4 gm; 78.8%) was ground and passed through a No. 20 mesh screen to produce 3,5-dichloro-4-hydroxy-N-(2-hydroxyethyl)benzamide as a cream colored solid (m.p. 174°-178° C.) which is suitable for use in the next step.
後処理
- temperatureThe resulting amber solution was heated to 145° C.
- distillationthe liberated methanol distilled into a Dean Stark trap
- customThe reaction required about 3.5 hrs
- temperatureUpon completion, the solution was cooled to 90°-100° C.
- temperatureThe aqueous solution was cooled to 25° C.
- customplaced in an ice bath
- customThe product precipitated
- filtrationfiltration
- customafforded a white solid
- customAfter drying at 50° C. in a vacuum oven
出典と根拠
- ORDレコード
- ord-0c537916309a471c85f0623899da2e0a
- 出典データセット
- uspto-grants-1991_03
- 特許番号
- US05002960
関連ノート
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