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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291737Generated: November 1, 2026

Triethylamine → HCID 54272040, compound

https://huagongshe.com/reaction/2291737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-BromoethanolHCID 10898—
Reactant1-Adamantanecarbonyl chlorideHCID 98915—
Reactant4-(Bis(4-fluorophenyl)methylene)piperidineHCID 2724436—
ReactantHCID 10660921HCID 10660921—
SolventDichloromethaneHCID 6344—
ProductHCID 54272040HCID 54272040—

Reaction Steps

To a stirred solution of 2-bromoethanol (4.9 g., 0.04 mol) in 50 mL of methylene chloride, adamantane-1-carboxylic acid chloride (5.6 g., 0.02 mol) and triethylamine (4 g., 0.04 mol) were added. The reaction mixture was stirred at room temperature overnight and the methylene chloride was washed with water, dried over anhydrous Na2SO4 and removed under reduced pressure to afford 12 g. of the intermediate adamantane-1-carboxylic acid bromoethyl ester. The title compound was prepared by stirring 4-[bis(4-fluorophenyl)-methylene]piperidine (2 g., 0.07 mol), adamantane-1-carboxylic acid bromoethyl ester (2.0 g., 0.007 mol) and triethylamine (1 g., 0.01 mol) in 50 mL of CH2Cl2 for 24 hours. The methylene chloride was washed with water, dried (anhydrous Na2SO4) and removed under reduced pressure. The remaining residue was subjected to preparative HPLC over silica gel using ethylacetate as the eluent and the desired product (TLC Rf = 0.75 in 30% ethanol/ethylacetate system) was separated and converted to the hydrochloride salt with ethanolic HCl; mp. 249°-254° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797489
Source datasetuspto-grants-1989_01
ORD IDord-fc7952648cce4a048e696f8544446ca0
Source noteuspto-grants-1989_01