Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3-[(Dimethylarsanyl)sulfanyl]valine | HCID 135080 | — |
| Reactant | HCID 13931490 | HCID 13931490 | — |
| Reactant | HCID 15020099 | HCID 15020099 | — |
| Reactant | HCID 18945828 | HCID 18945828 | — |
| Reactant | HCID 19915425 | HCID 19915425 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Cobalt | HCID 104730 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 86745326 | HCID 86745326 | — |
Reaction Steps
Into a 300 ml autoclave was placed 10 g of Raney cobalt and 15 g of anhydrous ammonia. A heel of 30 ml of t-butanol was then pumped into the reactor and the reactor heated externally to 90° C. The pressure was then raised to 850 psig with hydrogen. The crude product mixture containing bis(2-cyanoethoxy)ethane and DMAPN from Example 1 was then pumped into the autoclave at a rate of 0.6 g/min until 150 g of the mixture had been admitted. During the addition, the temperature was maintained at 90° C. and the pressure at 850 psig. Following the addition, the reactor was stirred an additional 1 hr until hydrogen uptake was complete. Analysis of the product mixture by GC (t-butanol free basis) revealed the composition to be 21.5 wt % DMAPA. 73.5 wt % of bis(3-aminopropoxy)ethane, 0.72 wt % of 3-aminopropoxyethanol, 1.2 wt % of N-(dimethylamino)-bis(3-aminopropoxy)ethane and 3.1 wt % of bis(aminopropoxyethoxypropyl)amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05075507 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-e7144f18903947b793754b666c77287e |
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| Source note | uspto-grants-1991_12 |
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