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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360618Generated: November 1, 2026

Ammonium Chloride → HCID 66959152, compound

https://huagongshe.com/reaction/1360618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-fur-2-yl-2-oxoacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl esterHCID 66592053—
ReactantHCID 178478989HCID 178478989—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66959152HCID 66959152—

Reaction Steps

Cyclopentylmagnesium chloride, 0.0472 mol (23.6 ml of a solution 2M in ether) was added to a solution of 9.4 g (0.0377 mol) of 2-fur-2-yl-2-oxoacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl ester dissolved in 125 ml of THF, at −70° C. under a N2 atmosphere. The mixture was stirred at this temperature for 10 minutes, and then warmed to room temperature. After 16 h, the reaction mixture was treated with a saturated solution of ammonium chloride and extracted twice with ethyl acetate. The organic phases were combined, washed with water, and dried over MgSO4. After removal of the solvent, the oil obtained (7.5 g) was purified by chromatography on silica gel eluting with chloroform/methanol/ammonia 95:5:0.5. Appropriate fractions were combined and evaporated to obtain the two diastereomers: I-14a, I-14b

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879874B2
Source datasetuspto-grants-2011_02
ORD IDord-f6ae0bdac0004d35af8a6294f8aaba36
Source noteuspto-grants-2011_02