Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772184Generated: November 2, 2026

Hydrochloric Acid → HCID 89483049, compound

https://huagongshe.com/reaction/1772184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetonitrileHCID 6342—
ReactantHCID 131734663HCID 131734663—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89483049HCID 8948304987.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under nitrogen atmosphere, to a 1000 mL of reaction flask were added dried acetonitrile (15.54 mL, 298.6 mmol) and anhydrous THF (350 mL). The mixture was cooled to −78° C. To the mixture was slowly added n-butyl lithium (171 mL, 1.6 mol/L, 273.7 mmol). The resultant mixture reacted with stirring for 30 min at −78° C. A solution of the compound of Example 4A (65.51 g, 248.8 mmol) in THT (100 mL) was added. The reaction was further kept for 1 hr at −78° C. Then, the reaction was warmed to −20° C. for 30 min, and finally warmed to room temperature for 30 min. The reaction was stopped. Ethyl ether (100 mL) was added to the reaction system to dilute. Water (100 mL) was added for quenching the reaction. pH was adjusted with diluted hydrochloric acid to 3. The organic phase was washed with saturated saline, dried and concentrated. The concentrated organic phase was separated by column chromatography to give 59.5 g of the title compound as pale yellow liquid. Yield: 87.8%. MS (ESI): m/z 273 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249172B2
Source datasetuspto-grants-2016_02
ORD IDord-b24cdad2fbec42128da14161092d68bd
Source noteuspto-grants-2016_02