HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479049Generated: October 29, 2026
o-Fluorobenzaldehyde → HCID 89650060, compound
https://huagongshe.com/reaction/1479049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | HCID 73977794 | HCID 73977794 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 89650060 | HCID 89650060 | 60% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403835B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-cfac339751c14500a20e54900e53de7a |
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| Source note | uspto-grants-2016_08 |
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