Diethylamine → Chlorobis(diethylamino)phosphine

HRID 541162

반응식

HRID 541162 반응식
[P:1]([Cl:4])(Cl)Cl.[CH2:5]([NH:7][CH2:8][CH3:9])[CH3:6]>C(OCC)C>[Cl:4][P:1]([N:7]([CH2:8][CH3:9])[CH2:5][CH3:6])[N:7]([CH2:8][CH3:9])[CH2:5][CH3:6]

참가 물질

4

실험 절차

In a 300 ml three-necked flask equipped with a dropping funnel and a magnetic stirrer, 10.0 g (0.0728 mol) of phosphorus trichloride and 100 ml of anhydrous diethyl ether were charged at room temperature in a nitrogen gas atmosphere, and the mixture was cooled to 5° C. or less in an ice bath. While the resulting reaction mixture was stirred, 30.0 ml (0.291 mol) of diethylamine were slowly added dropwise to the reaction mixture over 3 hours. The resulting crystals were filtered off under pressure in a nitrogen gas atmosphere. After the crystals were washed with anhydrous diethyl ether three times, they were purified by vacuum-distillation (0.4 kPa, 77.8-78.2° C.), and 8.07 g of chlorobis(diethylamino)phosphine were obtained in the form of a transparent liquid; the yield was 53%.

후처리

  1. customIn a 300 ml three-necked flask equipped with a dropping funnel and a magnetic stirrer
  2. temperaturethe mixture was cooled to 5° C. or less in an ice bath
  3. customWhile the resulting reaction mixture
  4. filtrationThe resulting crystals were filtered off under pressure in a nitrogen gas atmosphere
  5. washAfter the crystals were washed with anhydrous diethyl ether three times, they
  6. distillationwere purified by vacuum-distillation (0.4 kPa, 77.8-78.2° C.)

출처 및 근거

ORD 기록
ord-e094eb63ae574f998603998d9ea6316b
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08871974B2

연결된 노트

불러오는 중…