Bis(trimethylsilyl)carbodiimide → HCID 178511904, compound

HRID 2096566Notes

Reaction equation

HRID 2096566 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][CH:7]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:6][C:5]2=O.C[Si]([N:23]=[C:24]=[N:25][Si](C)(C)C)(C)C>C(Cl)Cl.Cl[Ti](Cl)(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][CH:7]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:6]/[C:5]/2=[N:25]\[C:24]#[N:23]

Participants

5

Procedure

To a solution of 6-bromo-2-phenylchroman-4-one (1.016 g, 3.35 mmol) in anhydrous DCM under N2 atmosphere was added 1 M TiCl4 (in DCM, 6.7 mL, 6.7 mmol) dropwise within 15 min at room temperature. The mixture was stirred for 1 h after the addition. To this mixture was added bis-trimethylsilylcarbodiimide (1.374 g, 7.37 mmol) dropwise. The resulting mixture was stirred for another 24 h after the addition. The reaction mixture was poured into ice-water (100 g), stirred for a while and filtered through a pad of Celite. The filtrate was extracted with DCM (3×30 mL). The combined organic phases were dried over anhydrous Na2SO4, filtered, and concentrated to give (E)-N-(6-bromo-2-phenylchroman-4-ylidene)cyanamide as light brown solid (899 mg), which was used in the next step without further purification. MS ESI +ve m/z 327 (M+H)+.

Workup

  1. additionafter the addition
  2. stirringThe resulting mixture was stirred for another 24 h
  3. additionafter the addition
  4. stirringstirred for a while
  5. filtrationfiltered through a pad of Celite
  6. extractionThe filtrate was extracted with DCM (3×30 mL)
  7. dry with materialThe combined organic phases were dried over anhydrous Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-0abba98d7c474b3fa7680322f94cd511
Source dataset
uspto-grants-2013_05
Patent number
US08450308B2

Reaction notes

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