HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Hydroxide → Tetrabutylammonium
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Reactant | 2-Amino-6-iodopurine | HCID 6101575 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tetrabutylammonium | HCID 16028 | — |
| Product | 2-Amino-6-iodopurine | HCID 6101575 | — |
Reaction Steps
To a mixture of 6-iodo-2-aminopurine (1.21 g., 4.637 mmole) in methylene chloride (12 ml.) at room temperature, was added 1.5M tetra(n-butyl)ammonium hydroxide (2.7 ml., 4.05 mmole). The reaction mixture was stirred for 10 minutes, and the volatiles were removed in vacuo. Methylene chloride (12 ml.) was added to the white residue, and the resulting solution was dried (magnesium sulfate), filtered, and the filtrate was concentrated in vacuo to yield the tetra(n-butyl)ammonium salt of 6-iodo-2-aminopurine as a white residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05414000 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-b08e4d29c6fd4228ab53668cb15e5f1a |
| Source note | uspto-grants-1995_05 |