تفاعل #3058

ord-428799f362c448f9a4b5974ac3fa405b

معادلة التفاعل

NC1CCCCCC1
cycloheptylamine
CCN(C(C)C)C(C)C
diisopropylethylamine
O=C(Br)CBr
bromoacetyl bromide
O=C(CBr)NC1CCCCCC1
solid
المردود 89.7%
O=C(CBr)NC1CCCCCC1
Bromo-N-cycloheptyl acetamide
المردود 89.7%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTo a -20° C.
  2. 2
    workup.STIRRINGstirred for an additional 30 minutes
  3. 3
    أخرىThe organic layer was separated
  4. 4
    غسيلwashed with water (3×100 mL)
  5. 5
    تجفيفdried over magnesium sulfate
  6. 6
    تركيزconcentrated in vacuo

الإجراء التجريبي

To a -20° C. solution of cycloheptylamine (6.37 mL, 50.0 mmol) and diisopropylethylamine (9.58 mL, 55.0 mmol) in methylene chloride (250 mL) was slowly added bromoacetyl bromide (4.78 mL, 55.0 mmol). The reaction mixture was warmed to room temperature over 20 minutes and stirred for an addition 30 minutes. The reaction mixture was diluted with water (100 mL) and stirred for an additional 30 minutes. The organic layer was separated, washed with water (3×100 mL), dried over magnesium sulfate and concentrated in vacuo to afford a beige solid (10.5 g). The crude material was further purified by silica gel flash column chromatography using hexane-ethyl acetate (1:1) as the eluent to give the purified title compound as a whim solid (9.77 g, 83%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05731438uspto-grants-1998_03