Triisopropylsilyl chloride → HCID 90303362, compound

HRID 1051966Notes

Reaction equation

HRID 1051966 reaction equation
[Li]CCCC.Br[C:7]1[S:11][CH:10]=[N:9][C:8]=1[O:12][CH2:13][CH:14]1[CH2:16][O:15]1.[CH3:17][CH:18]([Si:20](Cl)([CH:24]([CH3:26])[CH3:25])[CH:21]([CH3:23])[CH3:22])[CH3:19]>C1COCC1>[CH:18]([Si:20]([CH:24]([CH3:26])[CH3:25])([CH:21]([CH3:23])[CH3:22])[C:10]1[S:11][C:7]2[CH:14]([CH2:16][OH:15])[CH2:13][O:12][C:8]=2[N:9]=1)([CH3:19])[CH3:17]

Participants

5

Conditions

Temperature
-78 °C

Procedure

At −78° C., a soln. of n-BuLi in hexanes (2.18 M, 16.7 mL, 36.4 mmol) was added over 30 min to a soln. of 5-bromo-4-(oxiran-2-ylmethoxy)thiazole (7.17 g, 30.4 mmol) in THF (564 mL). The mixture was stirred at −78° C. for 2 h, then, TIPSCl (6.63 mL, 31.0 mmol) was added, the mixture was allowed to warm to RT and stirred at RT for 30 min. Subsequently, the mixture was cooled to −78° C. and treated with a soln. of n-BuLi in hexanes (2.18 M, 13.9 mL, 30.4 mmol). The mixture was stirred at 0° C. for 2 h, then, it was quenched with aq. sat. NaHCO3 and extracted with EtOAc. The comb. org. layers were washed with brine, dried over MgSO4, and conc. in vacuo. The residue was purified by means of CC (5-50% EtOAc/Hept) to provide a yellow oil.

Workup

  1. customAt −78° C.
  2. temperatureto warm to RT
  3. stirringstirred at RT for 30 min
  4. temperatureSubsequently, the mixture was cooled to −78° C.
  5. additiontreated with a soln
  6. stirringThe mixture was stirred at 0° C. for 2 h
  7. customit was quenched with aq. sat. NaHCO3
  8. extractionextracted with EtOAc
  9. washlayers were washed with brine
  10. dry with materialdried over MgSO4
  11. customThe residue was purified by means of CC (5-50% EtOAc/Hept)
  12. customto provide a yellow oil

Sources & evidence

ORD record
ord-d52183082f014c9a8a15766da8102e46
Source dataset
uspto-grants-2016_07
Patent number
US09388198B2

Reaction notes

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