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

HRID 2224326
Notes
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Reaction equation

HRID 2224326 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

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.

Workup

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

Sources & evidence

ORD record
ord-2b9fccb231af4938886b01cdecbb3f03
Source dataset
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07378426B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes