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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752318Generated: October 28, 2026

Sodium hydride → 2-Adamantyl 4-((2-methoxy-2-oxoethoxy)methyl)-4-phenylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1752318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl bromoacetateHCID 60984—
Reactant2-Adamantyl 4-(hydroxymethyl)-4-phenylpiperidine-1-carboxylateHCID 58171593—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-Adamantyl 4-((2-methoxy-2-oxoethoxy)methyl)-4-phenylpiperidine-1-carboxylateHCID 58171504130.8%

Reaction Steps

To a stirred solution of 2-adamantyl 4-(hydroxymethyl)-4-phenylpiperidine-1-carboxylate (230 mg, 0.62 mmol) in dry DMF (5 mL) was added 60% NaH in oil (60 mg, 2.5 mmol). The mixture was stirred at rt for 0.5 h and methyl bromoacetate (0.24 mL, 2.5 mmol) was added. The mixture was stirred at 50° C. in an oil bath for 4 h. The mixture was diluted with ether (90 mL), washed with water (3×20 mL), dried over MgSO4 and concentrated to leave an oil (358 mg). This material was purified by column chromatography on silica gel, eluted with an EtOAc in hexanes gradient, followed by prep HPLC to afford the title compound (20 mg, 7%) as an oil. LC-MS Method 2 tR=11.79 min, m/z=442.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163012B2
Source datasetuspto-grants-2015_10
ORD IDord-87bea2927fb3439e8f5c3a5b152c25fd
Source noteuspto-grants-2015_10