Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707934Generated: October 30, 2026

Sodium hydride → HCID 18960404, compound

https://huagongshe.com/reaction/1707934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 86621—
ReactantHCID 18960407HCID 18960407—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 18960404HCID 1896040486.9%

Reaction Steps

A solution of 5.0 g (0.020 mol) of N-(1,1-dimethylethyl)-1H-indole-3-sulfonamide in 30 mL anhydrous DMF was cooled to 10° C. under nitrogen atmosphere and was treated slowly with 0.87 g (0.022 mol) 60% sodium hydride (oil dispersion). The mixture was stirred for 20 minutes at room temperature then recooled to 10° C., whereupon 5.0 g (0.024 mol) of 2-(2'-bromoethoxy)tetrahydropyran (J. Org. Chem., Vol. 50, p. 4243, 1985) was added followed by heating to 70° C. for 3 hours. After cooling in an ice bath, 20 mL of saturated NH4Cl solution plus 20 mL of water was added and the mixture was extracted twice with ethyl acetate. The organic extract was washed twice with dilute HCl solution, then brine followed by drying (MgSO4) and evaporation in vacuo. The residue was triturated and collected by filtration with n-butyl chloride to afford 6.61 g of the title compound, m.p. 125°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356862
Source datasetuspto-grants-1994_10
ORD IDord-f35556a727024349a2a5ad029fd0fe6e
Source noteuspto-grants-1994_10