HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 73212385, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | HCID 16784433 | HCID 16784433 | — |
| Product | HCID 73212385 | HCID 73212385 | — |
Reaction Steps
3-Adamantan-1-yl-4-hydroxybenzoic acid (0.286 g), N-hydroxysuccinimide (0.12 g) and N,N′-dicyclohexylcarbodiimide (0.22 g) are dissolved in dioxane (5 mL) and stirred for 12 hours. The produced solid is filtered and the filtrate is added dropwise to a mixture solution of 3,4-dihydroxybenzylamine bromate (0.25 g), sodium bicarbonate (0.09 g) and water (1 mL). After stirring at 50° C. for 2 hours, the solution is cooled to room temperature, neutralized with 10% HCl solution and washed with ethyl acetate (30 mL). The organic layer is dried with anhydrous magnesium sulfate, filtered, concentrated under reduced pressure and separated by column chromatography to obtain 0.03 g of the target compound as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09254251B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-3bbb8b319e424e5ea73daea4df9068d3 |
| Source note | uspto-grants-2016_02 |