HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (1-Cyclohexylcarbamoylmethyl-cyclohexyl)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | 1,1-Cyclohexanediacetic Anhydride | HCID 2734289 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1-Cyclohexylcarbamoylmethyl-cyclohexyl)-acetic acid | HCID 43235048 | 115.9% |
Reaction Steps
A mixture of 1,1-cyclohexanediacetic anhydride (0.911 g, 5.0 mmol) and cyclohexylamine (0.63 mL, 5.5 mmol) in dichloromethane (10.0 mL) was stirred overnight at room temperature. The reaction mixture was diluted with H2O (5 mL) and the aqueous layer was acidified to pH-5 using 6 N HCl. The organic layer was collected. The aqueous layer was extracted with additional dichloromethane (5 mL). The organic extracts were combined, dried with sodium sulfate, filtered and concentrated to dryness to give crude title compound (1.63 g, 95% purity). (m/z): [M+H]+ calcd for C16H27NO3, 282.21. Found 282.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08497287B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-7ac9be8c538f42b0b9e09dfeb77da495 |
| Source note | uspto-grants-2013_07 |