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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium borohydrideHCID 4311764—
ReactantN-[2-(1-adamantyl)ethyl]-1-pentylamideHCID 86596070—
Product2-(2-hydroxyethoxy)acetic acid N-[2-(1-adamantyl)ethyl]-1-pentylamideHCID 5748127422%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741346B2
Source datasetuspto-grants-2010_06
ORD IDord-6ed94ec4435249158514bf72f8c4a981
Source noteuspto-grants-2010_06