تفاعل #2446073

ord-c9e3e0c6940a4200a840ed8e73edc87f

معادلة التفاعل

ClCCl
CH2Cl2
C[Si](C)(C)Cl
TMSCl
ClCCl
CH2Cl2
CCN(CC)CC
triethylamine
C[Si](C)(C)N(CCCCl)[Si](C)(C)C
ClCH2CH2CH2N(SiMe3)2
المردود 77.3%

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added slowly over 2 h
  2. 2
    أخرىto return to ambient temperature
  3. 3
    workup.STIRRINGwas stirred for 3 days
  4. 4
    أخرىThe supernatant liquid was decanted
  5. 5
    أخرىall volatile components were remove in vacuo
  6. 6
    أخرىto produce both a solid residue
  7. 7
    استخلاصThe liquid was extracted
  8. 8
    أخرىsubsequently the volatile components were removed under reduced pressure

الإجراء التجريبي

In a first step a 500 mL flask was charged with 13.002 g (100 mmol) of [ClCH2CH2CH2NH3]Cl that was dissolved in 300 mL of CH2Cl2 and 46.4 mL (300 mmol) of triethylamine. After ca. 10 min, a precipitate began to evolve. The flask was cooled to 0° C. and a solution containing 28.2 mL (222.2 mmol) of TMSCl and 50 mL of CH2Cl2 was added slowly over 2 h. The solution was stirred for an additional 2 h and then allowed to return to ambient temperature where it was stirred for 3 days. The supernatant liquid was decanted and then all volatile components were remove in vacuo to produce both a solid residue and a liquid. The liquid was extracted using ca. 200 mL of hexanes and subsequently the volatile components were removed under reduced pressure to yield 18.3898 g (77.30 mmol, 77.3%) of ClCH2CH2CH2N(SiMe3)2 as a colorless liquid. The product had the following NMR features: 1H NMR (300 MHz, CD3CN) δ=0.11 (s, —Si(CH3)3, 18H), 1.83 (m, CH2N, 2H, JHH=5.29 Hz), 3.52 (t, ClCH2, 2H, JHH=6.3 Hz); 13C{1H} NMR (75 MHz, CD3CN) 2.30, 38.50, 43.74, 43.93.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08685364B2uspto-grants-2014_04