Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047447Generated: October 31, 2026

Triethylamine → HCID 58356020, compound

https://huagongshe.com/reaction/2047447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 57537425HCID 57537425—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 58356020HCID 5835602096%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of (3R,4R)-1-(tert-butoxycarbonyl)-3-(4-fluoro-2-methylphenyl)piperidine-4-carboxylic acid (4.33 g) synthesized by a known method (WO2006/004195) in toluene (24 mL) were added DPPA (5.30 g) and triethylamine (2.7 mL) at room temperature, and the mixture was stirred at 100° C. for 1 hr. The reaction solution was cooled, 8N aqueous sodium hydroxide solution (16 mL) was added, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (NH Chromatorex) (solvent gradient; 30→70% ethyl acetate/hexane) to give the title compound (3.79 g, 96%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592454B2
Source datasetuspto-grants-2013_11
ORD IDord-09f14e6b49974d4ab53dee6516669b39
Source noteuspto-grants-2013_11