HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994281Generated: October 30, 2026
Sodium Hydroxide → 1-(Pentanoylamino)cyclopentane-1-carboxylic acid
https://huagongshe.com/reaction/1994281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Valeryl chloride | HCID 61186 | — |
| Reactant | Cycloleucine hydrochloride | HCID 3021985 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(Pentanoylamino)cyclopentane-1-carboxylic acid | HCID 16726891 | — |
Reaction Steps
In a 3 necked 250 ml round bottom flask equipped with mechanical stirrer, was charged with sodium hydroxide solution (24.1 g dissolved in 100 ml water) and 1-aminocyclopentane carboxylic acid hydrochloride (25 g) and chilled to 0° C. under stirring. Tetra butyl ammonium bromide (0.25 g) was added to the reaction mixture followed by slow addition of a solution of valeroyl chloride (27.5 g) in toluene (20 ml) during one hour at 0-5° C. under stirring. The reaction mass was stirred for 1 hour at 0-5° C. The reaction mixture was diluted with water (100 ml) toluene (20 ml) and stirred for 15 minutes. The two phases were separated. The aqueous phase was washed with toluene (20 ml). Aqueous phase was chilled to 10° C. and acidified with hydrochloric acid and stirred it for 1 hour. The product was filtered and washed with water. The product was dried at 60° C. till constant weight. (Yield: 22 g; 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652147B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-55cab2ef9d60477b972ce6cfefe1a5a6 |
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| Source note | uspto-grants-2010_01 |
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