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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530926Generated: October 25, 2026

Ammonium Chloride → HCID 66587953, compound

https://huagongshe.com/reaction/530926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(4-Bromobutoxy)tetrahydro-2H-pyranHCID 559019—
ReactantLithium diisopropylamideHCID 2724682—
Reactanttert-Butyl cyclopropanecarboxylateHCID 13676038—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 66587953HCID 6658795348.9%

Reaction Conditions

Temperature-65 °C

Reaction Steps

Under the argon atmosphere, tert-butyl cyclopropylcarboxylate (3.76 g) and 2-(4-bromobutoxy)tetrahydro-2H-pyran (7.52 g) were dissolved in anhydrous/THF (106 mL), followed by cooling to an inner temperature of −65° C. A lithium diisopropylamide solution (2.0M, THF:heptane:ethylbenzene solution) (19.8 mL) was added dropwise over 15 minutes. After completion of addition, the mixture was stirred at room temperature for 8 hours. An aqueous saturated ammonium chloride solution was added to stop the reaction, and water, and hexane:ethyl acetate (1:1) were added, followed by extraction. The organic layer was washed with dilute hydrochloric acid, water and an aqueous saturated sodium chloride solution, and dried with anhydrous sodium sulfate. The residue obtained by concentration was purified by silica gel column chromatography (hexane:ethyl acetate, 98:2→90:10) to obtain the title compound (3.86 g) having the following physical property values.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353113B2
Source datasetuspto-grants-2016_05
ORD IDord-8a9d3c6b9d004ceab18b43b791ed9aa9
Source noteuspto-grants-2016_05