Cyclopentadiene → Bicyclo(2.2.1)hept-5-ene-2-carbonyl chloride

HRID 229318

반응식

HRID 229318 반응식
[CH:1]1[CH2:5][CH:4]=[CH:3][CH:2]=1.[C:6]([Cl:10])(=[O:9])[CH:7]=[CH2:8]>>[CH:2]12[CH2:1][CH:5]([CH:7]([C:6]([Cl:10])=[O:9])[CH2:8]1)[CH:4]=[CH:3]2

참가 물질

3

반응 조건

온도
0 °C

실험 절차

A 1-L, three-neck round-bottom flask equipped with a magnetic stirrer, digital thermometer, glass stopper, an addition funnel with a nitrogen gas purge, and a dry-ice cooling bath was charged with freshly distilled cyclopentadiene (248 g, 3.75 mol), which was cooled to 0° C. The addition funnel was charged with freshly distilled acryloyl chloride (317 g, 3.5 mol), which was added drop wise to the reaction over about three hours while maintaining the reaction temperature between 0-10° C. After the acryloyl chloride addition was complete, the cooling bath was removed and the reaction allowed to warm to room temperature overnight. The reaction mixture was distilled under vacuum, collecting 533 g of the title product distilling at 54-56° C. at a pressure of 300 milliTorr.

후처리

  1. customdigital thermometer, glass stopper, an addition funnel with a nitrogen gas purge
  2. additionwas added drop
  3. customwise to the reaction over about three hours
  4. temperaturewhile maintaining the reaction temperature between 0-10° C
  5. customthe cooling bath was removed
  6. temperatureto warm to room temperature overnight
  7. distillationThe reaction mixture was distilled under vacuum
  8. customcollecting 533 g of the title product
  9. distillationdistilling at 54-56° C. at a pressure of 300 milliTorr

출처 및 근거

ORD 기록
ord-a721d469489b4148ab97b072f45581ba
출처 데이터셋
uspto-grants-2009_07
특허 번호
US07563558B2

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