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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734383Generated: November 1, 2026

Triethylamine → HCID 57845344, compound

https://huagongshe.com/reaction/734383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 57845345HCID 57845345—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57845344HCID 5784534491%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a suspension of crude acid (±)-((cis)-3-fluoro-1-{[(4-methylbenzyl)oxy]carbonyl}piperidin-4-yl)acetic acid (9.1 g, 29.4 mmol) in toluene (80 mL) was added triethylamine (10.2 mL, 73.5 mmol) and diphenylphosphoryl azide (9.52 mL, 44.1 mmol). The reaction mixture was heated to 70° C. and stirred for 20 min. A mixture of dioxane (80 mL) and 1 M NaOH (80 mL) was added and the reaction mixture was cooled to RT. The reaction mixture was concentrated to remove the dioxane and extracted with EtOAc three times, dried over Na2SO4, filtered and concentrated. The residue was suspended in CH2Cl2, stirred for 30 min, and the white preciptate filtered off. The filtrate was concentrated to give crude product (7.5 g) as a yellow oil, used directly in the next step. An analytical sample was purified by silica gel chromatography (gradient elution: CH2Cl2 to 80:20:2 CH2Cl2:MeOH:NH4OH) for characterization:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592360B2
Source datasetuspto-grants-2009_09
ORD IDord-4fa7ef47e3844e8a957c1b6a4be4f05c
Source noteuspto-grants-2009_09