Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Lithium amide | HCID 24532 | — |
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Reactant | HCID 14403133 | HCID 14403133 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14403135 | HCID 14403135 | 83.4% |
Reaction Steps
1 g 3-cyclopropylmethyl-9,9-dimethyl-3,7-diazabicyclo[3,3,1]nonane was dissolved in 25 ml absolute tetrahydrofuran, and 0.2 g lithium amide was added to the solution and stirred for 1 hour at 60° C. and then left to cool. After cooling, a solution of 3 g diphenylmethyl bromide in 25 ml absolute tetrahydrofuran was added slowly in drops, and the reaction mixture was stirred further for 90 min at a temperature of 40° C. Then the reaction mixture was acidified with aqueous citric acid solution and worked up as described in Example 1. 1.5 g 7-diphenylmethyl-3-cyclopropylmethyl-9,9-dimethyl-3,7-diazabicyclo[3,3,1]nonane were obtained as an oleaginous base.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04912113 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-3dfd5eef88dd4e419de26f9988b249d6 |
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| Source note | uspto-grants-1990_03 |
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