Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903133Generated: October 31, 2026

1,4-Dioxane → HCID 20468250, compound

https://huagongshe.com/reaction/1903133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 20468247HCID 20468247—
SolventWaterHCID 962—
ProductHCID 20468250HCID 2046825098.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 10 g of the product of Step A, 300 ml of dioxane and 5 g of N-chlorosuccinimide was stirred at 20° C. for 20 hours and was then diluted with water. The mixture was extracted with ethyl acetate and the organic phase was washed with water and aqueous sodium chloride solution, was dried and evaporated to dryness. The residue was chromatographed over silica gel and was eluted with a 6-3-1 cyclohexane-chloroform-triethylamine mixture to obtain 11 g of 3-chloro-4-(1-trifluoroacetyl-piperidin-3-yl)-1H-indole which was used as is for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435408
Source datasetuspto-grants-1984_03
ORD IDord-0a348002e3c34217b41975a878454d9b
Source noteuspto-grants-1984_03