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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479020Generated: November 1, 2026

2,4-Difluorobenzaldehyde → 3-(5-Fluoro-2-formyl-phenoxy)-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1479020

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluorobenzaldehydeHCID 73770—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
ReactantHCID 178418922HCID 178418922—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-(5-Fluoro-2-formyl-phenoxy)-azetidine-1-carboxylic acid tert-butyl esterHCID 8965017434%

Reaction Steps

tBuOK (948 mg; 8.44 mmol; 1.2 eq.) was added to a solution of 3-hydroxy-azetidine-1-carboxylic acid tert-butyl ester (1.46 g; 8.44 mmol; 1.2 eq.) in 1,4-dioxane (5 mL) and the solution was stirred at room temperature for 15 minutes whereupon a solution of 2,4-difluoro-benzaldehyde (1 g; 7.04 mmol; 1 eq.) in 1,4-dioxane (5 mL) was added dropwise. The reaction mixture was stirred at room temperature for 5 minutes then diluted with water. The solution was extracted with DCM (2×) and the combined organic phase was dried over magnesium sulfate and concentrated in vacuo. Purification by column chromatography (heptanes/EA) afforded the title compound (705 mg, 34%) as a white solid. 1H NMR (300 MHz, CDCl3) δ 10.41 (d, J=0.8 Hz, 1H), 7.93 (dd, J=8.7, 6.8 Hz, 1H), 6.99-6.72 (m, 1H), 6.33 (dd, J=10.2, 2.2 Hz, 1H), 5.07-4.85 (m, 1H), 4.40 (ddd, J=9.9, 6.4, 1.1 Hz, 2H), 4.10 (ddd, J=9.9, 4.0, 1.1 Hz, 2H), 1.48 (s, 9H). HPLC (max plot) 96.4%; Rt 4.22 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403835B2
Source datasetuspto-grants-2016_08
ORD IDord-73ad553d460944c8b211a4c2ef53df5f
Source noteuspto-grants-2016_08