HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789806Generated: November 2, 2026
Potassium Hydroxide → 2-(6-Tert-butoxycarbonylamino-pyridin-3-ylmethyl)-malonic acid monoethyl ester
https://huagongshe.com/reaction/1789806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(6-Tert-butoxycarbonylamino-pyridin-3-ylmethyl)-malonic acid diethyl ester | HCID 54480643 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(6-Tert-butoxycarbonylamino-pyridin-3-ylmethyl)-malonic acid monoethyl ester | HCID 53717796 | 50% |
Reaction Steps
A solution of KOH (0.37 g, 6.54 mmol) in ethanol (5 mL) was added to a solution of 2-(6-tert-butoxycarbonylamino-pyridin-3-ylmethyl)-malonic acid diethyl ester (2.18 g, 5.95 mmol) in ethanol (25 mL) and methylene chloride (10 mL) at 0° C. The mixture was stirred for 18 h at room temperature. The mixture was concentrated under reduced pressure and the residue dissolved in water. The aqueous layer was washed with ether, acidified to pH 4 by 1M HCl and extracted with methylene chloride. The organic layer was washed with water, brine and dried. After filtration and concentration under reduced pressure, the crude product was purified by flash chromatography (methanol/CH2Cl2, 1:20) to yield 2-(6-tert-butoxycarbonylamino-pyridin-3-ylmethyl)-malonic acid monoethyl ester (1.00 g, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071175B1 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-dcc7ced14d924601a79f1709878a8ac1 |
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| Source note | uspto-grants-2006_07 |
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