HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111247Generated: November 1, 2026
Cyclopentanone → (Rac)-3-cyclopentylamino-butanoic acid ethyl ester
https://huagongshe.com/reaction/2111247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Ethyl 3-aminobutyrate | HCID 98103 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (Rac)-3-cyclopentylamino-butanoic acid ethyl ester | HCID 57635031 | 50.2% |
Reaction Steps
To a solution of 1.5 g (0.010 mole) of (rac)-3-amino-butanoic acid ethyl ester (90% technical grade) and 0.93 mL (0.0105 mole) of cyclopentanone in 50 mL of dichloromethane was added 1.8 g (0.022 mole) of sodium acetate and 3.18 g (0.015 mole) of sodium triacetoxyborohydride. The mixture was stirred overnight at room temperature and then 50 mL of 10% sodium bicarbonate solution was added. The aqueous layer was extracted twice with 50 mL of dichloromethane and then combined dichloromethane layers were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with dichloromethane-methanol (100:0-95:5 gradient) to give 1.0 g of (rac)-3-cyclopentylamino-butanoic acid ethyl ester as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517873B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-6c83e7fb0c3d4f0293903ab0c908439b |
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| Source note | uspto-grants-2009_04 |
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