HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020758Generated: October 26, 2026
Guanidine Hydrochloride → HCID 135493693, compound
https://huagongshe.com/reaction/1020758
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Ethyl 3-cyclopentyl-3-oxopropanoate | HCID 11159709 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 135493693 | HCID 135493693 | 87.6% |
Reaction Steps
To a solution of 3-cyclopentyl-3-oxo-propionic acid ethyl ester (5.0 g, 27.4 mmol) and guanidine hydrochloride (3.1 g, 33.0 mmol) in MeOH (50 mL) at 23° C. was added potassium tert-butoxide, portionwise (16.7 g. 149 mmol) over 15 min with vigorous stirring and the reaction warmed to 60° C. The reaction was cooled to room temperature (rt) and stirred overnight and the precipitated salt was removed by filtration. The solution was concentrated to approximately 10 mL then diluted with 10 mL of water and adjusted to pH=5 by the addition of 6.0 N HCl (6.1 mL). The resulting precipitate was filtered and dried via suction then vacuum to yield a white solid (4.3 g, 87%) that was used without further purification. 1H NMR (MeOD): 10.71-10.54 (m, 1H), 6.58-6.32 (m, 2H), 5.44-5.37 (m, 1H), 2.66 (p, J=8.1, 1H), 1.91-1.73 (m, 2H), 1.72-1.48 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716475B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-acdce82425e740b7bf5c627129baeddd |
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| Source note | uspto-grants-2014_05 |
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