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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclobutanoneHCID 14496—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Azabicyclo(3.1.0)hexane-6-carboxylic acid, ethyl esterHCID 3522274—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-cyclobutyl-3-azabicyclo[3.1.0]hexane-6-carboxylateHCID 8672491166%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079894B2
Source datasetuspto-grants-2015_07
ORD IDord-49be979df04a4e8cad0929c40dccd61a
Source noteuspto-grants-2015_07