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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885045Generated: October 31, 2026

Triethylamine → HCID 178476687, compound

https://huagongshe.com/reaction/1885045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcetyl bromideHCID 10482—
ReactantHCID 154041398HCID 154041398—
SolventDichloromethaneHCID 6344—
ProductHCID 178476687HCID 17847668760.2%

Reaction Steps

(E)-1-(4-methanesulfonyl-benzylidene)-3,4-dihydro-1H-naphthalene-2-one oxime (25 mg, 0.076 mmol) and acetylbromide (0.017 ml, 0.23 mmol) were added into dichloromethane (2.0 ml). Then, at room temperature triethylamine (0.032 ml, 0.23 mmol) was added, stirred for an hour so as to complete the reaction. Afterward, an organic layer was separated by blending water, washed again with water and saturated brine, and then dried over anhydrous magnesium sulfate. The resulting solution was concentrated under reduced pressure and made to crystal by using a mixed organic solvent (diethylether/isopropanol/n-hexane=1/1/5, v/v/v). As a result, 16.9 mg of the present compound (productive yield 60%) was obtained as a white solid crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06768019B2
Source datasetuspto-grants-2004_07
ORD IDord-b0200488d9b7484b9b44ff92d40d1b2a
Source noteuspto-grants-2004_07