تفاعل #45665

ord-7114c87529a548ad8d6885f843c342be

معادلة التفاعل

CC(C)(C)[Si](Cl)(c1ccccc1)c1ccccc1
tert-butylchlorodiphenylsilane
CNCCO
N-methylethanolamine
c1c[nH]cn1
imidazole
CNCCO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
compound
المردود 39.0%
CNCCO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
[2-(tert-Butyldiphenylsiloxy)ethyl]methylamine
المردود 39.0%

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent was evaporated away under reduced pressure
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
  3. 3
    غسيلthe solution was washed with saturated sodium hydrogencarbonate water, water and saturated brine
  4. 4
    تجفيفNext, the organic layer was dried over anhydrous magnesium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    تركيزthe filtrate was concentrated under reduced pressure

الإجراء التجريبي

Under nitrogen atmosphere, an N,N-dimethylformamide (33 ml) solution of tert-butylchlorodiphenylsilane (8.78 g, 32.0 mmol) was dropwise added at room temperature to an N,N-dimethylformamide (100 ml) solution of N-methylethanolamine (2.00 g, 26.6 mmol) and imidazole (2.72 g, 39.9 mmol), and stirred for 5.5 hours. The solvent was evaporated away under reduced pressure, then the residue was dissolved in ethyl acetate, and the solution was washed with saturated sodium hydrogencarbonate water, water and saturated brine. Next, the organic layer was dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography, and the eluate with ethyl acetate gave the entitled compound (3.21 g, 39%) as a pale yellow oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07737166B2uspto-grants-2010_06