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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915262Generated: October 25, 2026

Ammonium Chloride → 3-Benzyl-4-hydroxy-4-methyl-3-azabicyclo[3.1.0]hexan-2-one

https://huagongshe.com/reaction/915262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Benzyl-3-azabicyclo(3.1.0)hexane-2,4-dioneHCID 2764586—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-Benzyl-4-hydroxy-4-methyl-3-azabicyclo[3.1.0]hexan-2-oneHCID 69121520—

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-benzyl-3-azabicyclo[3.1.0]hexane-2,4-dione (Prepared as per U.S. Pat. No. 4,183,857, 1.9 gm, 9.5 mmol) was dissolved in 100 ml of tetrahydrofuran and cooled to −78° C. Methyllithium (10.5 ml of a 0.98M solution in ether, 10.2 mmol) was added dropwise. Saturated aqueous ammonium chloride was added to the cold reaction mixture. The mixture was then extracted with ethyl acetate. The combined organic layers were dried over sodium sulphate, filtered and concentrated in vacuo to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265147B2
Source datasetuspto-grants-2007_09
ORD IDord-ab0a013d415a4bc682ea8d38df4f5433
Source noteuspto-grants-2007_09