HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 21433874, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-Morpholin-4-Yl-Butyric Acid Hydrochloride | HCID 12733746 | — |
| Reactant | HCID 21433882 | HCID 21433882 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21433874 | HCID 21433874 | — |
Reaction Steps
1.0 g. (3.5 mmoles) of 4,4-dimethyl-9-hydroxy-7-(phenyl-1-methylbutyl)-1,2,3,4-tetrahydrocyclopenta[c][1]benzopyran, 0.76 g. (3.63 mmoles) of γ-morpholinobutyric acid hydrochloride and 0.76 g. (3.70 mmoles) of dicyclohexylcarbodiimide are combined in 75 ml. of methylene chloride and stirred at room temperature for 24 hours. The insoluble by-product of dicyclohexylurea is removed by filtration and the methylene chloride solution is concentrated to 20 ml. Cyclohexane is added until the desired compound is obtained as a colorless solid. Recrystallization from methylene chloride/cyclohexane gives the desired crystalline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04025630 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-54dfccdf86e9408584c35e70b2ae52f0 |
| Source note | uspto-grants-1977_05 |