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Water → Tri-tert-butylphosphonium Tetraphenylborate

HRID 13869
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HRID 13869 반응식
[C:1]1([B-:7]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Na+].O.Cl.[C:29]([P:33]([C:38]([CH3:41])([CH3:40])[CH3:39])[C:34]([CH3:37])([CH3:36])[CH3:35])([CH3:32])([CH3:31])[CH3:30]>C1(C)C=CC=CC=1>[C:20]1([B-:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1.[C:38]([PH+:33]([C:29]([CH3:32])([CH3:31])[CH3:30])[C:34]([CH3:37])([CH3:36])[CH3:35])([CH3:39])([CH3:40])[CH3:41]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 2723787Sodium Tetraphenylborate2회HCID 23136656Tri-tert-butylphosphine hydrochloride

생성물 1

HCID 23136663Tri-tert-butylphosphonium Tetraphenylborate

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
25 °C

실험 절차

A 300-ml four-necked flask was equipped with a stirrer, a thermometer and a reflux condenser. 15.1 g (44 mmol) of sodium tetraphenylborate and 60 ml of water were weighed in the flask, followed by stirring to dissolve sodium tetraphenylborate. While the stirring was continuously carried out, the aqueous solution of tri-tert-butylphosphine hydrochloride was added to the solution, and the mixture was stirred at 25° C. for 3 hours. After the completion of the reaction, the precipitated product was filtered off. The so obtained crystal was suspended in 100 ml of toluene at 50° C., and the suspension was cooled to 25° C. and filtered. The product filtered off was washed with 100 ml of toluene. The crystal was then suspended in 100 ml of methanol at 50° C., and the suspension was cooled to 25° C. and filtered. The product filtered off was washed with 100 ml of methanol. The crystal obtained was dried to give 18.2 g of objective tri-tert-butylphosphonium tetraphenylborate as white crystal. The yield (mol %) was 87% based on tri-tert-butylphosphine.

후처리

  1. customA 300-ml four-necked flask was equipped with a stirrer
  2. stirringthe mixture was stirred at 25° C. for 3 hours
  3. customAfter the completion of the reaction
  4. filtrationthe precipitated product was filtered off
  5. customThe so obtained crystal
  6. filtrationfiltered
  7. filtrationThe product filtered off
  8. washwas washed with 100 ml of toluene
  9. customwas then suspended in 100 ml of methanol at 50° C.
  10. temperaturethe suspension was cooled to 25° C.
  11. filtrationfiltered
  12. filtrationThe product filtered off
  13. washwas washed with 100 ml of methanol
  14. customThe crystal obtained
  15. customwas dried

출처 및 근거

ORD 기록
ord-dddf007533ea440ba2297d1c746f5899
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728176B2

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