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

HRID 1169628
ノート
印刷プレビュー

反応式

HRID 1169628 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 222387192,6-Dichloro-4-hydroxybenzoic acid

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
-78 °C

実験手順

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.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-d96e77bfcd7f4d05a6d007d68b57906a
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07825121B2

反応ノート

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