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

HRID 1169628
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HRID 1169628 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

HCID 222387192,6-Dichloro-4-hydroxybenzoic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
-78 °C

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-d96e77bfcd7f4d05a6d007d68b57906a
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07825121B2

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