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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479049Generated: October 29, 2026

o-Fluorobenzaldehyde → HCID 89650060, compound

https://huagongshe.com/reaction/1479049

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-FluorobenzaldehydeHCID 67970—
ReactantHCID 73977794HCID 73977794—
ReactantHCID 178418922HCID 178418922—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 89650060HCID 8965006060%

Reaction Conditions

Temperature50 °C

Reaction Steps

tBuOK (136 mg; 1.21 mmol; 1.5 eq.) was added to a solution of 4-hydroxy-3-trifluoromethyl-piperidine-1-carboxylic acid tert-butyl ester (239 mg; 0.89 mmol; 1.1 eq.) in 1,4-dioxane (10 mL) and the reaction mixture was stirred at 50° C. for 15 minutes. After cooling down to room temperature, 2-fluoro-benzaldehyde (100 mg; 0.81 mmol; 1 eq.) was added and the reaction was stirred at 50° C. for 30 minutes. The solution was diluted with water and extracted with EA (3×). The combined organics were dried over magnesium sulfate and concentrated in vacuo. Purification by column chromatography (10% to 30% EA in heptane) afforded the title compound (181 mg, 60%) as colourless oil. HPLC (max plot) 99.9%, Rt 5.02 min. UPLC/MS: (MS+) 274.2 ([M-(Boc)+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403835B2
Source datasetuspto-grants-2016_08
ORD IDord-cfac339751c14500a20e54900e53de7a
Source noteuspto-grants-2016_08