HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508481Generated: October 28, 2026
Ammonium Chloride → HCID 58153490, compound
https://huagongshe.com/reaction/508481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 58153355 | HCID 58153355 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58153490 | HCID 58153490 | 89.2% |
Reaction Steps
In a 10 ml single-necked round-bottomed flask equipped with an efficient condensor, 2-bromo-5-chloro-6-(4-methyl-pentyloxy)-3-nitro-pyridine (200 mg) is dissolved in dry acetonitrile (3.00 ml). To the reulting yellow solution, copper(I) cyanide (109 mg) is added. The resulting suspension is stirred under heating to reflux for 6 hours whereupon a brown solution is obtained. The progress of the transformation is followed by GC-MS. The mixture is allowed to reaxch ambient temperature. Saturated ammonium chloride solution (20 ml) along with some ice is then added and the mixture extracted with ether (2×20 ml). The combined organic phases are then dried over sodium sulfate, filtered and the solvent is removed in vacuo to give 150 mg of the title compound in the form of a yellow oil (89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096525B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-0d7aad0ce8f6479cb4995103c5923a39 |
|---|
| Source note | uspto-grants-2015_08 |
|---|