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Phosphorus pentachloride → 2-Chloro-5-nitrobenzo[d]oxazole

HRID 1886935
Notes
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Reaction equation

HRID 1886935 reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:11][C:10](=S)[NH:9][C:8]=2[CH:13]=1)([O-:3])=[O:2].P(Cl)(Cl)(Cl)(Cl)[Cl:15]>P(Cl)(Cl)(Cl)=O>[Cl:15][C:10]1[O:11][C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:13][C:8]=2[N:9]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24819Phosphorus pentachlorideHCID 7862935-Nitrobenzo[D]Oxazole-2-Thiol

Product 1

HCID 103527232-Chloro-5-nitrobenzo[d]oxazole

Reagents, catalysts & solvents 1

HCID 24813Phosphorus oxychlorideSolvent

Conditions

Temperature
100 °C

Procedure

To a solution of 5-nitrobenzo[d]oxazole-2(3H)-thione (2.52 g, 12.86 mmol) in phosphorous oxychloride (21 mL) was added phosphorous pentachloride (2.68 g, 12.86 mmol) in one portion. The mixture was then heated to 100° C. for 2.5 h. After cooling, the excess of phosphorous oxychloride was removed in vacuo and the resulting mixture was used crude without characterisation.

Workup

  1. temperatureAfter cooling
  2. customthe excess of phosphorous oxychloride was removed in vacuo

Sources & evidence

ORD record
ord-3dc15de79c7642018c0bb348cb65dd34
Source dataset
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08501713B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes