HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (4-Azidophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Nitrate | HCID 24268 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 4-Aminobenzyl alcohol | HCID 69331 | — |
| Reactant | HCID 178483607 | HCID 178483607 | — |
| Product | (4-Azidophenyl)methanol | HCID 11171062 | 55% |
Reaction Steps
For example, 4-azidobenzylphosphorylcholine was made as follows: 4-aminobenzyl alcohol was treated with HCl and reacted with sodium nitrate, followed by sodium azide to yield 4-azidobenzyl alcohol. The product was recovered in 55% yield as a brown solid and purified by column chromatography. The product was characterized by NMR and IR. 4-azidobenzyl alcohol was treated with triethylamine, and 2-chloro-2-oxo-1,3,2-dioxaphospholane (COP) was added to the solution. The resulting compound was reacted with trimethylamine to yield the final product of 4-azidobenzylphosphorylcholine. The final product was obtained as a pale brown powder in 60% yield and characterized by NMR and IR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802738B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-ae3c66eb7d444598b864460096b3b863 |
| Source note | uspto-grants-2014_08 |