HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzene-1-carboximidamide hydrochloride → HCID 12535814, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzene-1-carboximidamide hydrochloride | HCID 203436 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Diethyl ethoxypropanedioate | HCID 12196926 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12535814 | HCID 12535814 | — |
Reaction Steps
Sodium ethoxide (11.12 ml, 2 equiv) as a 21% w/v solution in ethanol was added dropwise to a suspension of diethyl ethoxymalonate (3.03 ml, 1 equiv) and 4-chlorobenzamidine hydrochloride (4.23 g, 1 equiv) in ethanol (30 ml), then the mixture was heated to reflux for 4 hours. After cooling, the solvent was removed in vacuo and the residue was triturated with ether. The solid was filtered off, then resuspended in water and acidified to pH 2. The product was filtered off, washed with water and dried; yield 2.94 g. 1H-NMR (d6-DMSO) δ 1.29 (3H, t), 4.26 (2H, q), 7.65 (2H, m), 8.18 (2H, m), 8.65 (1H, s); MS (APCI−) found (M−1) =277/279; C13H11ClN2O3 requires 278/280.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153861B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-b226588bc20c46fda7bd737bb6af7151 |
| Source note | uspto-grants-2006_12 |