Hydrochloric Acid → HCID 10083450, compound

HRID 1762654Notes

Reaction equation

HRID 1762654 reaction equation
[C:1]1(=[O:11])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH2:2]1.[CH:12](=O)[C:13]1[C:14](=[CH:16][CH:17]=[CH:18][CH:19]=1)[OH:15].CC(C)([O-])C.[K+].Cl>C(O)(C)(C)C>[OH:15][C:14]1[CH:16]=[CH:17][CH:18]=[CH:19][C:13]=1[CH2:12][C:2]1[CH:3]=[CH:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[C:1]=1[OH:11]

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 6998SalicylaldehydeHCID 107241-TetraloneHCID 23665647Potassium tert-butoxide

Product 1

HCID 10083450HCID 10083450, compoundYield 52.3%

Reagents, catalysts & solvents 1

HCID 6386tert-ButanolSolvent

Procedure

A solution of 1-tetralone (5.85 g, 0.040 mole) and salicylaldehyde (4.88 g, 0.040 mole) in t-butanol (400 mL) was treated with potassium t-butoxide (17.6 g, 0.160 mole) was heated at reflux for 16 hours. After cooling to room temperature, the solution was poured into stirred 1.0N hydrochloric acid. After isolation by extraction with ethyl acetate, the crude product was chromatographed with 4:1 petroleum ether/ether, to provide a tan solid. This was recrystallized (cyclohexane/chloroform) to give the titel compound as white needles (5.24 g, 52%), mp 124°-125°.

Workup

  1. temperaturewas heated
  2. temperatureat reflux for 16 hours
  3. additionthe solution was poured
  4. extractionAfter isolation by extraction with ethyl acetate
  5. customthe crude product was chromatographed with 4:1 petroleum ether/ether
  6. customto provide a tan solid
  7. customThis was recrystallized (cyclohexane/chloroform)

Sources & evidence

ORD record
ord-b69223cf2d6b42c681aab1b8b1918ac2
Source dataset
uspto-grants-1989_05
Patent number
US04833164

Reaction notes

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