Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223931Generated: October 26, 2026

Sodium Bicarbonate → 2-[1-[2-[4-(p-Toluidino)piperidin-1-yl]ethyl]cyclooctyl]ethanol

https://huagongshe.com/reaction/2223931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(4-Methylphenyl)-4-piperidinamineHCID 23020914—
Reactant3-Oxaspiro[5.7]tridecan-2-olHCID 59714915—
Solvent1,2-DichloroethaneHCID 11—
SolventTriethylamineHCID 8471—
Product2-[1-[2-[4-(p-Toluidino)piperidin-1-yl]ethyl]cyclooctyl]ethanolHCID 5971486445.5%

Reaction Steps

To a suspension of 4-(p-toluidino)piperidine ditrifluoroacetate (synthesized in Preparation Example 4-5) (1.31 g) in 1,2-dichloroethane (6 mL) was added triethylamine (0.96 mL). The suspension was stirred at room temperature for 5 minutes. Then, a solution of 3-oxaspiro[5.7]tridecan-2-ol (synthesized in Example 72) (0.62 g) in 1,2-dichloroethane (3 mL) was added to the suspension, and it was stirred at room temperature for additional 10 minutes. The reaction solution was ice-cooled and sodium triacetoxyborohydride (0.70 g) was added thereto. The reaction solution was then allowed for its temperature to rise to room temperature, and the solution was stirred for additional 4.5 hours. Saturated aqueous sodium bicarbonate solution was added to the reaction solution and it was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by chromatography [silica gel, methanol-chloroform (3:97 to 1:9)] to give the title compound (0.53 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375115B2
Source datasetuspto-grants-2008_05
ORD IDord-a33a41345cae424fa0c7a6b8c2d0cf29
Source noteuspto-grants-2008_05