HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18416Generated: October 30, 2026
Methanol → 2-(2-hydroxyethoxy)acetic acid N-[2-(1-adamantyl)ethyl]-1-pentylamide
https://huagongshe.com/reaction/18416
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[2-(1-adamantyl)ethyl]-1-pentylamide | HCID 86596070 | — |
| Product | 2-(2-hydroxyethoxy)acetic acid N-[2-(1-adamantyl)ethyl]-1-pentylamide | HCID 57481274 | 22% |
Reaction Steps
Next, sodium borohydride (0.18 g, 4.8 mmol) was added to a solution of N-[2-(1-adamantyl)ethyl]-1-pentylamide (0.37 g, 0.96 mmol) in methanol (3 ml) under ice-cooling, and the mixture was stirred at room temperature overnight. Water (10 ml) was added to the reaction mixture, and the whole was stirred for 10 minutes and then distributed between water (20 ml) and ethyl acetate (30 ml). The organic layer was washed with a saturated aqueous sodium chloride solution (10 ml) and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography to give 2-(2-hydroxyethoxy)acetic acid N-[2-(1-adamantyl)ethyl]-1-pentylamide (74 mg, 22%) as an oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07741346B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-6ed94ec4435249158514bf72f8c4a981 |
|---|
| Source note | uspto-grants-2010_06 |
|---|