HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220048Generated: October 29, 2026
Potassium tert-butoxide → 1-Acetyl-5-[4-(2,2-difluoroethyl)phenyl]piperidine-3-carboxylic acid
https://huagongshe.com/reaction/220048
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Methyl 1-acetyl-5-[4-(2,2-difluoroethyl)phenyl]piperidine-3-carboxylate | HCID 59606565 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Acetyl-5-[4-(2,2-difluoroethyl)phenyl]piperidine-3-carboxylic acid | HCID 59606579 | — |
Reaction Steps
410 mg (3.65 mmol) of potassium tert-butoxide were added at RT to a solution of 205 mg (0.365 mmol, purity 61%) of the compound from Example 58A in methanol (6.9 ml). The mixture was stirred at 60° C. overnight. For workup, the methanol was removed under reduced pressure, the residue was admixed with water and the mixture was acidified (pH 1) with aqueous 1 N hydrochloric acid solution. The mixture was extracted with ethyl acetate, and the organic phase was dried with magnesium sulphate, filtered and concentrated under reduced pressure. Yield: 153 mg (67% of theory, purity 50%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202862B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-f02235104ddc49259f89ec76b46f8cb5 |
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| Source note | uspto-grants-2012_06 |
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