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Aluminium lithium hydride → 4-(2-(4-(4-Hydroxybutyl)phenyl)ethoxy)quinazoline

HRID 1479235
Notes
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Reaction equation

HRID 1479235 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].C[O:8][C:9](=O)[CH2:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][O:21][C:22]2[C:31]3[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=3)[N:25]=[CH:24][N:23]=2)=[CH:15][CH:14]=1.CCCCC.C(OCC)(=O)C>C(OCC)C.ClCCl.[O-2].[Mn+4].[O-2]>[N:25]1[C:26]2[C:31](=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:22]([O:21][CH2:20][CH2:19][C:16]2[CH:15]=[CH:14][C:13]([CH2:12][CH2:11][CH2:10][CH2:9][OH:8])=[CH:18][CH:17]=2)=[N:23][CH:24]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 21226445Aluminium lithium hydrideHCID 22335286Ethyl acetate pentaneHCID 596786664-{4-[2-(Quinazolin-4-yloxy)ethyl]phenyl}butyric acid methyl ester

Product 1

HCID 444419894-(2-(4-(4-Hydroxybutyl)phenyl)ethoxy)quinazolineYield 49%

Reagents, catalysts & solvents 3

HCID 178418406
HCID 178418406, compound
Catalyst
HCID 3283Diethyl EtherSolvent2×
HCID 6344DichloromethaneSolvent

Procedure

To a dry 15 mL flask was added lithium aluminum hydride (233 mg, 6.0 mmol) and anhydrous diethyl ether (3 mL). The mixture was cooled with an ice bath. A solution of Example 1C (538 mg, 1.54 mmol) in anhydrous diethyl ether (3 mL) was slowly added with vigorous stirring. The bath was removed and the slurry was stirred for 15 minutes. The reaction was quenched with water (0.233 mL), aqueous 15% sodium hydroxide (0.233 mL) and water (0.699 mL). The white solid was filtered and the filtrate was dried over magnesium sulfate, filtered, and concentrated under reduced pressure to give a clear oil. The oil was then dissolved in anhydrous dichloromethane (10 mL) and manganese(IV) oxide (500 mg, 5.8 mmol) was added to the solution. The mixture was stirred for 12 hours. Filtration through diatomaceous earth (Celite®) followed by concentration of the filtrate under reduced pressure afforded 395 mg of crude product. Column chromatography [silica gel; eluent pentane-ethyl acetate (2:3)] provided the desired product (225 mg, 49%). 1H (CDCl3) δ(ppm): 1.55-1.61 (m, 2H); 1.65-1.68 (m, 2H); 2.61 (t, 2H); 3.17 (t, 2H); 3.64 (t, 2H); 4.79 (t, 2H); 7.12 (d, 2H); 7.23 (d, 2H); 7.56 (t, 1H); 7.82 (t, 1H); 7.93 (d, 1H); 8.14 (d, 1H); 8.77 (s, 1H). 13C (CDCl3) δ(ppm): 27.52, 32.31, 34.89, 35.21, 62.81, 67.74, 116.67, 123.54, 127.08, 127.49, 128.63, 128.98, 133.61, 135.23, 140.64, 150.68, 154.29, 166.79.

Workup

  1. temperatureThe mixture was cooled with an ice bath
  2. customThe bath was removed
  3. customThe reaction was quenched with water (0.233 mL), aqueous 15% sodium hydroxide (0.233 mL) and water (0.699 mL)
  4. filtrationThe white solid was filtered
  5. dry with materialthe filtrate was dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customto give a clear oil
  9. stirringThe mixture was stirred for 12 hours
  10. filtrationFiltration through diatomaceous earth (Celite®)
  11. customafforded 395 mg of crude product

Sources & evidence

ORD record
ord-430d16eaf901424ea6aed4589c030d98
Source dataset
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09408927B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes