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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291735Generated: October 31, 2026

Triethylamine → HCID 53700015, compound

https://huagongshe.com/reaction/2291735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Bis(4-fluorophenyl)methylene)piperidineHCID 2724436—
ReactantHCID 14373539HCID 14373539—
SolventDichloromethaneHCID 6344—
ProductHCID 53700015HCID 53700015—

Reaction Steps

To a stirred solution of 3-bromopropanol (5.5 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, 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 bromopropyl ester. The title compound was prepared by stirring 4-[bis(4-fluorophenyl)-methylene]piperidine (2 g, 0.07 mol), adamantane-1-carboxylic acid bromo-propyl ester (2.1 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 =0.7 in 30% ethanol/ethylacetate system) was separated and converted to the hydrochloride salt (0.6 g, 16% yield), mp. 267°-269° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797489
Source datasetuspto-grants-1989_01
ORD IDord-ed97d6615e744bdc9b28d3e7f371fc9e
Source noteuspto-grants-1989_01