関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 1,4-Dicyanobenzene | HCID 12172 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Cobalt | HCID 104730 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1,4-Benzenedimethanamine | HCID 68315 | — |
反応手順
A stirred autoclave was charged with 400 ml. tetrahydrofuran (THF), 100 ml. ammonia, 50 g. terephthalonitrile (TPN) and 6.0 g. cobalt supported catalyst and various amounts of water. The autoclave was heated to 120° C. Hydrogen was introduced rapidly until the selected pressure was reached. The absorption of hydrogen started immediately and additional hydrogen was added to keep the pressure at the selected level. The course of the reaction was monitored by measuring the volume of hydrogen consumed and by periodic withdrawal of a small sample of the reaction mixture for analysis. When the analysis indicated that all of the terephthalonitrile had reacted, the agitation was stopped and the reactor was cooled rapidly and vented. The reaction mixture was filtered to recover the catalyst and then was flash evaporated to remove solvent. The residual oil was flash distilled at about 100° C. and 0.5 mm Hg. to give practically pure p-xylylene diamine. A small amount of high boiling residue remained in the distillation pot. Results of experiments conducted with various amounts of water and at 1500 and 2500 psig are listed in Table I.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04222961 |
|---|
| 出典データセット | uspto-grants-1980_09 |
|---|
| ORD ID | ord-7e6cd9f6c5f9464fbaee0cb1ba972c3b |
|---|
| 出典メモ | uspto-grants-1980_09 |
|---|