Ammonium Chloride → 2-methyl-4-amino-N-tetrahydrofurfurylaniline dihydrochloride monohydrate
反応式
[Cl-:1].[NH4+].[CH3:3][C:4]1[CH:16]=[C:15]([N+:17]([O-])=O)[CH:14]=[CH:13][C:5]=1[NH:6][CH2:7][CH:8]1[O:12][CH2:11][CH2:10][CH2:9]1>[Zn]>[OH2:12].[ClH:1].[ClH:1].[CH3:3][C:4]1[CH:16]=[C:15]([NH2:17])[CH:14]=[CH:13][C:5]=1[NH:6][CH2:7][CH:8]1[O:12][CH2:11][CH2:10][CH2:9]1参加物
実験手順
5 g of ammonium chloride and 83 g of zinc powder are added to 250 ml of an aqueous-alcoholic solution (85% of alcohol and 15% of water). This mixture is heated to the reflux temperature, whilst stirring, and 0.168 mol (39.8 g) of 2-methyl-4-nitro-N-tetrahydrofurfurylaniline is then added gradually. When the addition of the nitro derivative has ended and the reaction medium is completely decolorised, the latter is filtered and the filtrate is collected in 40 ml of ice-cooled hydrochloric acid (d=1.19). 80 ml of acetone are added to the filtrate. 2-Methyl-4-amino-N-tetrahydrofurfurylaniline dihydrochloride precipitates in the form of the monohydrate. The crystalline product is filtered off and washed with absolute alcohol and then acetone. After drying in vacuo, it melts at about 210° C. with decomposition.
後処理
- temperatureThis mixture is heated to the reflux temperature
- filtrationthe latter is filtered
- customthe filtrate is collected in 40 ml of ice-
- temperaturecooled hydrochloric acid (d=1.19)
- addition80 ml of acetone are added to the filtrate
- custom2-Methyl-4-amino-N-tetrahydrofurfurylaniline dihydrochloride precipitates in the form of the monohydrate
- filtrationThe crystalline product is filtered off
- washwashed with absolute alcohol
- customAfter drying in vacuo, it melts at about 210° C. with decomposition
出典と根拠
- ORDレコード
- ord-adbbed078b494ba3ba30377556bc3e35
- 出典データセット
- uspto-grants-1979_04
- 特許番号
- US04149848
反応ノート
読み込み中…