HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907425Generated: October 30, 2026
Ammonium Chloride → HCID 178471100, compound
https://huagongshe.com/reaction/907425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Cyclopropanecarboximidamide hydrochloride | HCID 2781916 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 4,4-diethoxy-3-oxobutanoate | HCID 11138577 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178471100 | HCID 178471100 | 88% |
Reaction Steps
A portion (˜40.4 mL) of the ethanol solution of cyclopropanecarboximidamide monohydrochloride as prepared in Example 1 was added to a portion (˜210 mL) of the solution of the sodium salt of ethyl 4,4-diethoxy-3-oxobutanoate as prepared in Example 2. The mixture was allowed to stir overnight at room temperature. The mixture was boiled for about 2 h and then allowed to cool to room temperature. The mixture was evaporated under reduced pressure, and the residue was redissolved in toluene (200 mL). A solution of ammonium chloride (0.68 g, 12.7 mmol) in water (30 mL) was added. After stirring for 10 minutes, the aqueous phase was removed. The organic phase was dried and evaporated to leave the product as pale yellow solid (27.27 g, 88% yield). Product recrystallized from hexanes melted at 111.5-112.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08013155B2 |
|---|
| Source dataset | uspto-grants-2011_09 |
|---|
| ORD ID | ord-6a6468129f93470d837670f7f77be639 |
|---|
| Source note | uspto-grants-2011_09 |
|---|