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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736131Generated: October 25, 2026

Sodium hydride → HCID 19434808, compound

https://huagongshe.com/reaction/1736131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantTetrahydropyranyl etherHCID 263182—
Reactant6-Iodo-1-hexanolHCID 13089081—
ReactantHCID 19434956HCID 19434956—
SolventDimethylformamideHCID 6228—
ProductHCID 19434808HCID 1943480870%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.0 g (2.99 mmol) of Compound 38 obtained in Example 38 was dissolved in 20 ml of dimethylformamide under argon atmosphere, 239 mg of sodium hydride (60% oil dispersion) and 1.87 g of tetrahydropyranyl ether of 6-iodo-1-hexanol were added under ice-cooling and the mixture was stirred at 0° C. for 1.3 hours. An aqueous saturated solution of ammonium chloride was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated solution of sodium chloride and dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. 18 ml of ethanol and 2 ml of concentrated hydrochloric acid were added to the residue and the mixture was stirred at room temperature for 18 hours. The reaction solution was adjusted to pH 7 by addition of a 10N aqueous solution of sodium hydroxide thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated solution of sodium chloride and dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (chloroform: methanol=40:1) and recrystallized from n-hexane/ethyl acetate to give 912 mg (70%) of Compound 60.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05539112
Source datasetuspto-grants-1996_07
ORD IDord-7728e9370c704d789c187c494eef4db4
Source noteuspto-grants-1996_07