Water → HCID 131729337, compound

HRID 416203Notes

Reaction equation

HRID 416203 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5](Br)=[CH:4][N:3]=1.[CH2:9]([Li])[CH2:10][CH2:11][CH3:12].[CH:14]1([Si:20](C)([CH3:22])Cl)CCCCC1.O.[CH2:25](OCC)[CH3:26]>>[Br:1][C:2]1[C:7]([SiH:20]([CH3:22])[CH3:14])=[CH:6][C:5]([CH:9]2[CH2:26][CH2:25][CH2:12][CH2:11][CH2:10]2)=[CH:4][N:3]=1

Participants

6

Conditions

Temperature
-70 °C

Procedure

To a reaction container equipped with a dropping funnel, 24 g of 2,5-dibromopyridine and 270 ml of diethyl ether were added. The obtained solution was cooled at −70° C. and then, 62.93 mL of butyl lithium (1.61 M/hexane solution) was added dropwise thereto. The obtained mixture was stirred for 2 hours and then, a solution obtained by dissolving 18.75 mL of cyclohexyldimethylchlorosilane in 18.6 mL of diethyl ether was added dropwise thereto. The obtained mixture was stirred for 4 hours and then, 140 mL of water was added dropwise thereto at 0° C. The obtained mixture was stirred at room temperature overnight and then, 40 mL of water and 150 mL of diethyl ether were added thereto. The obtained solution was extracted three times with 150 mL of diethyl ether. The obtained organic layers were mixed and dried with magnesium sulfate. After removing magnesium sulfate by filtration, the filtrate was concentrated to obtain a crude product. The crude product was purified with silica gel column chromatography to obtain 23.0 g of 2-bromo-5-cyclohexyldimethylsilylpyridine. Purity: 93% (area percentage value obtained by gas chromatography analysis).

Workup

  1. customTo a reaction container equipped with a dropping funnel
  2. customa solution obtained
  3. additionwas added dropwise
  4. stirringThe obtained mixture was stirred for 4 hours
  5. customat 0° C
  6. stirringThe obtained mixture was stirred at room temperature overnight
  7. extractionThe obtained solution was extracted three times with 150 mL of diethyl ether
  8. additionThe obtained organic layers were mixed
  9. dry with materialdried with magnesium sulfate
  10. customAfter removing magnesium sulfate
  11. filtrationby filtration
  12. concentrationthe filtrate was concentrated
  13. customto obtain a crude product
  14. customThe crude product was purified with silica gel column chromatography

Sources & evidence

ORD record
ord-4f8ee3c7068d4aeeb3a5b469622aaabc
Source dataset
uspto-grants-2012_01
Patent number
US08088883B2

Reaction notes

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