Water → HCID 15523935, compound

HRID 1978008Notes

Reaction equation

HRID 1978008 reaction equation
[NH2:1][CH2:2][CH:3]=[C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([O:14][CH3:15])[CH:12]=2)[CH2:7][CH2:6][CH2:5]1.C(N(CC)CC)C.[C:23](Cl)(=[O:25])[CH3:24].O>C1COCC1>[C:23]([NH:1][CH2:2]/[CH:3]=[C:4]1\[CH2:5][CH2:6][CH2:7][C:8]2[C:13]\1=[CH:12][C:11]([O:14][CH3:15])=[CH:10][CH:9]=2)(=[O:25])[CH3:24]

Participants

6

Reactant 4

HCID 962WaterHCID 6367Acetyl chlorideHCID 8471TriethylamineHCID 54094556HCID 54094556, compound

Product 1

HCID 15523935HCID 15523935, compoundYield 40.2%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a solution of 1-(2-aminoethylidene)-7-methoxy-1,2,3,4-tetrahydronaphthalene (2.0 g, 9.74 mmol) and triethylamine (1.5 g, 14,6 mmol) in THF (20 ml) was gradually added dropwise, under ice-cooling, acetyl chloride (0.76 g, 9.74 mmol). The mixture was stirred for 30 minutes at room temperature. The reaction mixture was poured into water, and the organic layer was subjected to extraction with chloroform. The extract solution was washed with brine and water, which was dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (ethyl acetate), followed by recrystallization from ethyl acetate/hexane to give the above-titled compound (yield 0.96 g, 40%).

Workup

  1. temperaturecooling
  2. extractionthe organic layer was subjected to extraction with chloroform
  3. washThe extract solution was washed with brine and water, which
  4. dry with materialwas dried over anhydrous magnesium sulfate
  5. distillationThe solvent was then distilled off under reduced pressure
  6. customThe residue was purified by means of a silica gel column chromatography (ethyl acetate)
  7. customfollowed by recrystallization from ethyl acetate/hexane

Sources & evidence

ORD record
ord-198b743818f048838415d033a55e8fda
Source dataset
uspto-grants-2001_05
Patent number
US06235789B1

Reaction notes

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