HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N'-(acetyloxy)-4-iodobenzenecarboximidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Hydroxy-4-iodo-benzamidine | HCID 4429393 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | N'-(acetyloxy)-4-iodobenzenecarboximidamide | HCID 86663308 | — |
Reaction Steps
To a suspension of the product obtained in Step A above (8.43 g, 32.17 mmol) in 200 ml of CH2Cl2 there are added 6.72 ml (48.2 mmol) of triethylamine. 3.34 ml (35.4 mmol) of acetic anhydride are added dropwise and the solution is stirred overnight at ambient temperature. After washing 3 times with water and then with brine, the organic phase is dried over MgSO4 and evaporated. The solid obtained is taken up in isopropyl ether and then filtered to yield the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569285B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-8dc8ac9c5a664b2bb408d871c4126b8e |
| Source note | uspto-grants-2013_10 |