HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178476687, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | HCID 154041398 | HCID 154041398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178476687 | HCID 178476687 | 60.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06768019B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-b0200488d9b7484b9b44ff92d40d1b2a |
| Source note | uspto-grants-2004_07 |