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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373997Generated: October 30, 2026

Sulfuric acid magnesium salt (1:1) → F-15063

https://huagongshe.com/reaction/1373997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantPotassium borohydrideHCID 4192641—
ReactantHCID 12094928HCID 12094928—
ReactantHCID 16109477HCID 16109477—
Solvent1,2-DichloroethaneHCID 11—
ProductF-15063HCID 1024815951.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

1.5 g of magnesium sulfate are added to a solution of 3-cyclopenten-1-ylbenzaldehyde (2a) (0.56 g, 3.26 mmol) and of [2-(2,2-dimethyl-2,3-dihydrobenzofuran-7-yl-oxy)]ethylamine (3a) (0.68 g, 3.26 mmol) in 15 ml of 1,2-dichloroethane and the mixture is heated at 60° C. for 17 hours. The mixture is cooled to room temperature, the solid is filtered and the solvent is evaporated under reduced pressure. The residue is diluted with 15 ml of methanol and then cooled to 0° C. 0.35 g of potassium borohydride (6.52 mmol) is then introduced and the reaction mixture is stirred for 3 hours at 0° C. The mixture is then poured into ice-cold water, extracted with ethyl acetate and washed with a saturated aqueous sodium chloride solution. The combined organic phases are dried over magnesium sulfate, filtered and the solvent is evaporated under reduced pressure. The residue is purified by chromatography on silica gel (methylene chloride/methanol/aqueous ammonia: 98/1.5/0.5). The title product (0.61 g) is isolated in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163957B2
Source datasetuspto-grants-2007_01
ORD IDord-b74206b81c02401283790deccbea8468
Source noteuspto-grants-2007_01