Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | 2,6-Diaminotoluene | HCID 13205 | — |
| Reactant | HCID 68115044 | HCID 68115044 | — |
| Product | Isobutylene | HCID 8255 | — |
| Product | 2,3-Diaminotoluene | HCID 17593 | — |
Reaction Steps
Synthesis of the above recited ortho-tert-butyltoluenediamine (hereinafter 3tBTDA) was carried out in a 1 gallon stainless steel pressure vessel equipped with a mechanical stirrer. The vessel was charged with a 150 gram portion of a powdered commercially available silica-alumina catalyst containing 13% alumina and 1500 grams (12.24 moles of 2,6-toluenediamine. The autoclave was sealed and purged with nitrogen. A residual blanket of nitrogen was left in the autoclave, leaving the pressure at 16 psig. the contents of the reactor were heated to a temperature of 200° C. with constant agitation. Isobutylene was then introduced into the reactor and 870 grams or 15.5 moles were added over a 30 minute period resulting in an initial reaction of pressure of 970 psig. This provided a mole ratio of 1.26:1 isobutylene to toluenediamine. The reaction mixture was maintained at 200° C. for about 45 hours with constant agitation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04693837 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-7409e6c6e6334471b118efddca67ce8f |
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| Source note | uspto-grants-1987_09 |
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