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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482558Generated: November 3, 2026

Chloroform → HCID 86753046, compound

https://huagongshe.com/reaction/482558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Bromomethyl)-2,3-dihydro-1-benzofuranHCID 140637—
ProductHCID 86753046HCID 8675304667%

Reaction Steps

430 mg (2.0 mmol) of compound 001C, which had been prepared in Step C, was dissolved in 4 ml of acetonitrile. To the resultant solution were added 0.92 ml (10.0 mmol) of 4-amino-1-buthanol and 550 mg (4.0 mmol) of potassium carbonate and then, the resultant mixture was stirred at 80° C. for 8 hours to effect a reaction. To the resultant reaction mixture was added 20 ml of chloroform to obtain a mixture. The obtained mixture was successively washed with 20 ml of a saturated aqueous sodium hydrogencarbonate solution, 20 ml of water and 20 ml of saturated saline, to thereby form a chloroform layer containing the desired compound 001D, followed by separation of the chloroform layer. The chloroform layer thus separated was dehydrated by means of a Whatman 1PS filter paper and then, concentrated in vacuo to thereby obtain a residue. The obtained residue was purified by silica gel column chromatography. That is, the residue was applied to a column of 10 g of silica gel (Art. 9385, manufactured and sold by E. Merck, Darmstadt, Germany) and eluted with a mixed solvent of chloroform-methanol-concentrated aqueous ammonia (10:1:0.1), to thereby obtain 300 mg of compound 001D as a light yellow oily substance (yield: 67 %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798382
Source datasetuspto-grants-1998_08
ORD IDord-fb4ddb9439a7432cad2265d25f7b7c47
Source noteuspto-grants-1998_08