Hydrochloric Acid → HCID 14551714、化合物

HRID 359846

反応式

HRID 359846 の反応式
[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

5

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

  1. temperatureThe resulting amber solution was heated to 145° C.
  2. distillationthe liberated methanol distilled into a Dean Stark trap
  3. customThe reaction required about 3.5 hrs
  4. temperatureUpon completion, the solution was cooled to 90°-100° C.
  5. temperatureThe aqueous solution was cooled to 25° C.
  6. customplaced in an ice bath
  7. customThe product precipitated
  8. filtrationfiltration
  9. customafforded a white solid
  10. 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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