Aluminium lithium hydride → HCID 53798457, compound

HRID 1493050Notes

Reaction equation

HRID 1493050 reaction equation
[C:1]([NH:4][C:5]1[C:6]([CH3:26])=[C:7]([CH3:25])[C:8]2[O:12][C:11]([CH3:22])([CH2:13][CH2:14][C:15]3[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=3)[CH2:10][C:9]=2[C:23]=1[CH3:24])(=O)[CH3:2].[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[CH2:1]([NH:4][C:5]1[C:6]([CH3:26])=[C:7]([CH3:25])[C:8]2[O:12][C:11]([CH2:13][CH2:14][C:15]3[CH:16]=[CH:17][C:18]([F:21])=[CH:19][CH:20]=3)([CH3:22])[CH2:10][C:9]=2[C:23]=1[CH3:24])[CH3:2]

Participants

4

Reactant 2

HCID 21226445Aluminium lithium hydrideHCID 23358488HCID 23358488, compound

Product 1

HCID 53798457HCID 53798457, compoundYield 71.2%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To tetrahydrofuran (20 ml) were added 5-acetylamino-2,4,6,7-tetramethyl-2-[2-(4-fluorophenyl) ethyl]-2,3-dihydrobenzofuran (1.2 g, 3.4 mmol) and lithium aluminum hydride. The mixture was heated under reflux for 3 hours. The reaction mixture was poured into ice water and the product was extracted with ethyl acetate. The extract was washed with water and dried and then the solvent was distilled off. The residue was purified by column chromatography on silica gel (isopropyl ether-ethyl acetate, 2:1) to obtain the desired compound (0.82 g, yield: 71.2%}as oil.

Workup

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 3 hours
  3. extractionthe product was extracted with ethyl acetate
  4. washThe extract was washed with water
  5. customdried
  6. distillationthe solvent was distilled off
  7. customThe residue was purified by column chromatography on silica gel (isopropyl ether-ethyl acetate, 2:1)

Sources & evidence

ORD record
ord-16b1dec57c7849b39eafde7b2a6a6e7c
Source dataset
uspto-grants-1994_12
Patent number
US05376681

Reaction notes

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