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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417482Generated: October 31, 2026

Benzyl Bromide → HCID 57015605, compound

https://huagongshe.com/reaction/1417482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-(2,3,4,9-Tetrahydrothiopyrano[2,3-b]indol-2-yl)methyl-4,4-dimethyl-2-oxazolineHCID 54359105—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57015605HCID 57015605—

Reaction Steps

71 mg of 2-(2,3,4,9-tetrahydrothiopyrano[2,3-b]indol-2-yl)methyl-4,4-dimethyl-2-oxazoline (prepared as described in Example 80) in 1 ml of dimethylformamide was added to a suspension of 11 mg of sodium hydride (55% w/w dispersion in mineral oil) in 1 ml of dimethylformamide, with stirring and ice-cooling. Stirring was continued at this temperature for 30 minutes and then 0.03 ml of benzyl bromide was added to the reaction mixture, with stirring and ice-cooling. Stirring was continued for a further hour. At the end of this time, the reaction mixture was diluted with water and then extracted with ethyl acetate. The ethyl acetate fraction was then washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure and the resulting residue was purified by silica gel column chromatography, using a mixture of 20% v/v ethyl acetate in hexane as the eluent, to afford 71 mg of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877199
Source datasetuspto-grants-1999_03
ORD IDord-5dc7efb2110a4dc2a4b6fa6ebbe6137e
Source noteuspto-grants-1999_03