HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 69373404, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-Iodobenzohydrazide | HCID 615774 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69373404 | HCID 69373404 | — |
Reaction Steps
A solution of cyanogen bromide (1.06 g, 10.0 mmol) in 10 mL of methanol was added dropwise to an ice-cold suspension of 3-iodobenzhydrazide (2.62 g, 10.0 mmol, Intermediate 7, Step A) in 20 mL of methanol. After 30 min, the mixture was allowed to warm to room temperature and was then warmed at reflux for 1.5 h. The resultant solution was cooled to 0° C., and neutralized to pH 9 with concentrated aqueous ammonium hydroxide. The resultant precipitate was collected, washed with methanol, and dried in vacuo to afford the product as an off-white powder. LC/MS 288.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157490B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-5eb302d548784ab4b320fcfecb51b6d9 |
| Source note | uspto-grants-2007_01 |