HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523725Generated: November 3, 2026
Acetic Acid → Ethyl 3-cyclobutyl-3-azabicyclo[3.1.0]hexane-6-carboxylate
https://huagongshe.com/reaction/1523725
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Azabicyclo(3.1.0)hexane-6-carboxylic acid, ethyl ester | HCID 3522274 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-cyclobutyl-3-azabicyclo[3.1.0]hexane-6-carboxylate | HCID 86724911 | 66% |
Reaction Steps
A mixture of cyclobutanone (157 mg, 2.19 mmol) in acetic acid (0.11 mL, 1.56 mmol) was added to a stirred solution of ethyl 3-aza bicyclo[3.1.0]hexane-6-carboxylate (243 mg, 1.56 mmol, obtained in the above step) in dichloromethane, cooled at 0° C. Solid sodium triacetoxy borohydride (727 mg, 3.43 mmol) was added portion wise over a period of 15 minutes. The reaction mixture was gradually warmed to room temperature and stirred for 16 hours. The reaction mixture was cooled to 0° C. and basified with saturated sodium bicarbonate solution (pH: 7.5). The two layers were separated, the organic layer was washed with brine, dried over anhydrous sodium sulfate and the volatiles were removed under reduced pressure to obtain ethyl 3-cyclobutyl-3-aza bicyclo[3.1.0]hexane-6-carboxylate (219 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079894B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-49be979df04a4e8cad0929c40dccd61a |
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| Source note | uspto-grants-2015_07 |
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