Triphenylphosphine → 1-Bromo-3,5-di-tert-butylbenzene

HRID 842479

반응식

HRID 842479 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br:20]Br.[C:22]([C:26]1[CH:27]=[C:28](O)[CH:29]=[C:30]([C:32]([CH3:35])([CH3:34])[CH3:33])[CH:31]=1)([CH3:25])([CH3:24])[CH3:23]>C(#N)C>[Br:20][C:28]1[CH:27]=[C:26]([C:22]([CH3:25])([CH3:24])[CH3:23])[CH:31]=[C:30]([C:32]([CH3:35])([CH3:34])[CH3:33])[CH:29]=1

참가 물질

5

실험 절차

A 1000 mL three-neck, round-bottom flask was equipped with a mechanical stirrer, a pressure-compensating dropping funnel, and a reflux condenser. A nitrogen gas flow adapter with overpressure valve was attached on top of the reflux condenser. A slight nitrogen flow guaranteed an inert gas atmosphere in the apparatus. The flask was charged with 181 g triphenylphosphine (690 mmol) and 160 mL acetonitrile (HPLC grade). The white suspension was cooled in an ice bath for 15 minutes. While stirring, dropwise addition of 101.5 g bromine (635 mmol) took place within 40 minutes. After bromine addition, the ice bath was removed. 124 g of 3,5-di-tertbutylphenol (601 mmol) and 140 mL acetonitrile were added in one portion. The orange/white suspension converted into an orange solution upon heating. The mechanical stirrer was replaced by an egg-shape stir bar. The solution was stirred at gentle reflux temperature for three hours.

후처리

  1. customA 1000 mL three-neck, round-bottom flask was equipped with a mechanical stirrer
  2. customA nitrogen gas flow adapter with overpressure valve was attached on top of the reflux condenser
  3. temperatureThe white suspension was cooled in an ice bath for 15 minutes
  4. customwithin 40 minutes
  5. customthe ice bath was removed
  6. temperatureupon heating
  7. stirringstir bar
  8. stirringThe solution was stirred at gentle reflux temperature for three hours

출처 및 근거

ORD 기록
ord-8a4721adaa65478f8561016645ae4af0
출처 데이터셋
uspto-grants-2002_04
특허 번호
US06376412B1

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