تفاعل #487539

ord-af066d1ff502410bbe64e55a9b0bfefa

معادلة التفاعل

Cl
hydrochloric acid
CCCCCCCCCC(=O)N(C)OC
N-methoxy-N-methyldecanamide
[Mg]
magnesium
CCCCCCCCCBr
1-bromononane
CCCCCCCCCC(=O)CCCCCCCCC
10-nonadecanone
المردود 95.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated
  2. 2
    درجة الحرارةAfter heating
  3. 3
    درجة الحرارةto reflux for 1.5 hours
  4. 4
    أخرىobtained by the method
  5. 5
    استخلاصfollowed by extraction with diethyl ether two times
  6. 6
    workup.ADDITIONAnhydrous magnesium sulfate was added to the organic layer
  7. 7
    أخرىto dry it
  8. 8
    ترشيحthe resultant was filtrated
  9. 9
    تركيزwas then concentrated
  10. 10
    أخرىThe obtained residue was purified

الإجراء التجريبي

Polished shaved magnesium (3.2 g, 134 mmol) was heated, and thereafter, an anhydrous THF solution (68 ml) of 1-bromononane (12.9 ml, 67.5 mmol) was slowly added dropwise thereto. After heating to reflux for 1.5 hours, the reaction solution was cooled to a room temperature, and it was then added dropwise to a THF (80 mL) solution of the N-methoxy-N-methyldecanamide (4.8 g, 22.5 mmol) obtained by the method described in Production Example D-1-1. After the obtained mixture had been stirred for 30 minutes, 1 N hydrochloric acid was added to the reaction solution, followed by extraction with diethyl ether two times. Anhydrous magnesium sulfate was added to the organic layer to dry it, and the resultant was filtrated and was then concentrated. The obtained residue was purified using column chromatography (hexane:dichloromethane=8:1), so as to obtain 10-nonadecanone (6.0 g, 95%) as a ketone body in the form of a white amorphous solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08741871B2uspto-grants-2014_06