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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Boron tribromide → HCID 57925832, 화합물

HRID 1013457
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HRID 1013457 반응식
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([P:9]2(=[O:16])[CH2:14][CH2:13][N:12]([CH3:15])[CH2:11][CH2:10]2)=[CH:5][CH:4]=1.B(Br)(Br)Br>C(Cl)Cl>[CH3:15][N:12]1[CH2:13][CH2:14][P:9]([C:6]2[CH:7]=[CH:8][C:3]([OH:2])=[CH:4][CH:5]=2)(=[O:16])[CH2:10][CH2:11]1
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 57925863HCID 57925863, 화합물

생성물 1

HCID 57925832HCID 57925832, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-78 °C

실험 절차

4-(4-Methoxyphenyl)-1-methyl-1,4-azaphosphinane 4-oxide (1.05 g, 4.39 mmol) was made 0.16 M in DCM and stirred at −78° C. To this stirring solution was added BBr3 (2.09 g, 8.34 mmol) dropwise. The reaction mixture was slowly warmed to ambient temperature over 16 h. The precipitate was filtered off then dissolved in water. The pH was adjusted to pH=7 with 2N aq HCl. A precipitate was filtered off and the filtrate was concentrated in vacuo. The residue was suspended in 4:1 DCM:MeOH and stirred for 20 mins. The solids were filtered off and the filtrate was concentrated in vacuo to afford the requisite product. MS: cal'd 226 (MH+), exp 226 (MH+)

후처리

  1. temperatureThe reaction mixture was slowly warmed to ambient temperature over 16 h
  2. filtrationThe precipitate was filtered off
  3. dissolutionthen dissolved in water
  4. filtrationA precipitate was filtered off
  5. concentrationthe filtrate was concentrated in vacuo
  6. stirringMeOH and stirred for 20 mins
  7. filtrationThe solids were filtered off
  8. concentrationthe filtrate was concentrated in vacuo
  9. customto afford the requisite product

출처 및 근거

ORD 기록
ord-01f1dc3e80594ee7a757b14e6364dafc
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981874B2

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