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Boron tribromide → 2,6-Dichloro-4-hydroxybenzoic acid

HRID 1936596
Notes
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Reaction equation

HRID 1936596 reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]([O:11]C)[CH:8]=[C:7]([Cl:13])[C:3]=1[C:4]([OH:6])=[O:5].B(Br)(Br)Br>C(Cl)Cl>[Cl:1][C:2]1[CH:10]=[C:9]([OH:11])[CH:8]=[C:7]([Cl:13])[C:3]=1[C:4]([OH:6])=[O:5]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 25134Boron tribromideHCID 144847262,6-Dichloro-4-methoxybenzoic acid

Product 1

HCID 222387192,6-Dichloro-4-hydroxybenzoic acid

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Conditions

Temperature
-78 °C

Procedure

2,6-Dichloro-4-methoxy-benzoic acid (500 mg, 2.3 mmol) was taken up in CH2Cl2 and cooled to −78° C. BBr3 (6.9 ml of a 1 M solution in CH2Cl2) was added to the solution at −78° C. The solution was warmed to 25° C. and stirred at that temperature for 16 h. The solution was quenched with 3 N NaOH. The aqueous layer was extracted with CH2Cl2. The aqueous layer was cooled (0° C.) and acidified with conc. HCl (pH=1-2). The aqueous layer was extracted with CH2Cl2. The combined organic layers were dried (Na2SO4). Filtration and concentration gave the crude phenol which was used without further purification.

Workup

  1. temperatureThe solution was warmed to 25° C.
  2. customThe solution was quenched with 3 N NaOH
  3. extractionThe aqueous layer was extracted with CH2Cl2
  4. temperatureThe aqueous layer was cooled (0° C.)
  5. extractionThe aqueous layer was extracted with CH2Cl2
  6. dry with materialThe combined organic layers were dried (Na2SO4)
  7. filtrationFiltration and concentration

Sources & evidence

ORD record
ord-6ff00e9b38dd40829c2e10b8bdd02210
Source dataset
uspto-grants-2002_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06391865B1

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes