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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523724Generated: November 4, 2026

Ethyl 3-benzyl-2,4-dioxo-3-azabicyclo[3.1.0]hexane-6-carboxylate → Ethyl 3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylate

https://huagongshe.com/reaction/1523724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-benzyl-2,4-dioxo-3-azabicyclo[3.1.0]hexane-6-carboxylateHCID 15713436—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylateHCID 1581845762.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of ethyl 3-benzyl-2,4-dioxo-3-aza bicyclo[3.1.0]hexane-6-carboxylate (SYNLETT, 1996, 1097; 5.0 grams, 18.3 mmol) in tetrahydrofuran (74 mL) cooled at 0° C., BH3-DMS (2N solution in tetrahydrofuran 36 mL, 73.2 mmol) was added over a period of 30 minutes. The reaction temperature was gradually raised to reflux for 6 hours. After cooling the reaction mixture to 0° C., it was quenched by adding aqueous ammonium chloride solution and was extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulphate and the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography to obtain ethyl 3-benzyl-3-aza bicyclo[3.1.0]hexane-6-carboxylate (2.8 grams)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079894B2
Source datasetuspto-grants-2015_07
ORD IDord-240e4f757abf4ee3af472c74400d59d9
Source noteuspto-grants-2015_07