Water → HCID 17968139, compound

HRID 1767768Notes

Reaction equation

HRID 1767768 reaction equation
[H-].[H-].[H-].[H-].[Li+].[Al+3].[C:7]([Si:11]([CH3:25])([CH3:24])[O:12][C:13]1[C:21]2[O:20][C:19]([CH2:22]Cl)=[CH:18][C:17]=2[CH:16]=[CH:15][CH:14]=1)([CH3:10])([CH3:9])[CH3:8].O>O1CCCC1.CN(C)C=O.C(O)(C)C>[C:7]([Si:11]([CH3:25])([CH3:24])[O:12][C:13]1[C:21]2[O:20][C:19](=[CH2:22])[CH2:18][C:17]=2[CH:16]=[CH:15][CH:14]=1)([CH3:10])([CH3:9])[CH3:8]

Participants

7

Procedure

LiAlH4 (1.0M in tetrahydrofuran, 4.5 ml, 4.5 mmol) is added dropwise to a suspension of CrCl3 (1.4 g, 8.85 mmol) in tetrahydrofuran (10 ml), kept at 0° C. and the mixture is stirred for 15 minutes. The solution is then diluted with dimethylformamide (18 ml) and isopropanol (1.35 ml). tert-Butyldimethyl-(2-chloromethylbenzofuran-7-yloxy)silane (15) (1.05 g, 3.54 mmol) in dimethylformamide (15 ml) is added to the solution obtained, kept at 0° C. The mixture is stirred at room temperature for 18 hours and then poured into water and extracted with pentane. The organic phase is dried over Na2SO4, filtered and concentrated under reduced pressure. A colorless liquid is obtained (0.78 g) which is used in the next step without further purification.

Workup

  1. customkept at 0° C.
  2. customobtained
  3. customkept at 0° C
  4. stirringThe mixture is stirred at room temperature for 18 hours
  5. extractionextracted with pentane
  6. dry with materialThe organic phase is dried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customA colorless liquid is obtained (0.78 g) which
  10. customis used in the next step without further purification

Sources & evidence

ORD record
ord-c0b7f6ec0bc14bbab9466195165521a4
Source dataset
uspto-grants-2007_06
Patent number
US07235568B2

Reaction notes

Loading…