4-Methoxybenzaldehyde → 4-Methoxybenzyl alcohol

HRID 1484228Notes

Reaction equation

HRID 1484228 reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[CH:5][CH:4]=1.C[Si](C)(C)O[SiH](C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1COCC1>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([CH2:7][OH:8])=[CH:5][CH:4]=1

Participants

5

Procedure

A 30-mL eggplant flask equipped with a magnetic stirrer was heat dried while pumping to a vacuum of 5 Pa before its interior was purged with nitrogen atmosphere. To the flask, 4-methoxybenzaldehyde (140 mg, 1.0 mmol) and 1,1,1,3,3-pentamethyldisiloxane (371 mg, 2.5 mmol) were added through a syringe, and iron complex A (5 mg, 0.01 mmol) was admitted as catalyst. The solution was stirred at room temperature for 3 hours. At 0° C., THF (1 mL) and tetrabutylammonium fluoride in THF (1 M, 1 mL) were then added to the solution, which was stirred at 0° C. for 1 hour. THF was distilled off in vacuum. The crude product was purified by silica gel-packed column chromatography using hexane/ethyl acetate (3/1) as developing solvent, obtaining 4-methoxybenzyl alcohol (131 mg, 0.95 mmol, 95%). The results as are shown as Entry 2 in Table 6. The resulting alcohol was identified for geometry by 1H and 13C-NMR spectroscopy.

Workup

  1. customA 30-mL eggplant flask equipped with a magnetic stirrer
  2. temperaturewas heat
  3. customdried
  4. customwas purged with nitrogen atmosphere
  5. stirringwas stirred at 0° C. for 1 hour
  6. distillationTHF was distilled off in vacuum
  7. customThe crude product was purified by silica gel-

Sources & evidence

ORD record
ord-3f249b2001d04e2a8c61362b066d2135
Source dataset
uspto-grants-2016_08
Patent number
US09421532B2

Reaction notes

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