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Dichloromethane → 4-Bromomethyl-3-iodo-pyridine hydrobromide

HRID 2224326
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HRID 2224326 반응식
[I:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH2:8]O.P(Br)(Br)[Br:11].C(Cl)Cl>C1COCC1>[BrH:11].[Br:11][CH2:8][C:7]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[I:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6344DichloromethaneHCID 24614Phosphorus tribromideHCID 23106621(3-Iodopyridin-4-yl)methanol

생성물 1

HCID 692909234-Bromomethyl-3-iodo-pyridine hydrobromide수율 171.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 24A (142 mg, 0.604 mmol) and PBr3 (0.61 mL, 1M in CH2Cl2, 0.61 mmol) in THF (5 mL) was heated to reflux for 30 minutes. The reaction mixture was cooled to room temperature, CH2Cl2 was added and the mixture was filtered. The solid was rinsed with CH2Cl2 and dried to give 24B (198.2 mg, 86.6%). HPLC Rt=1.756 min.

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 30 minutes
  3. filtrationthe mixture was filtered
  4. washThe solid was rinsed with CH2Cl2
  5. customdried

출처 및 근거

ORD 기록
ord-2b9fccb231af4938886b01cdecbb3f03
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07378426B2

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