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Methanol → Methyl 2-bromo-3-chlorobenzoate

HRID 1481361
ノート
印刷プレビュー

反応式

HRID 1481361 の反応式
[Br:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH3:16]O>C(Cl)Cl.CN(C=O)C>[CH3:16][O:5][C:4](=[O:6])[C:3]1[CH:7]=[CH:8][CH:9]=[C:10]([Cl:11])[C:2]=1[Br:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 331232-Bromo-3-chlorobenzoic acid

生成物 1

HCID 53751442Methyl 2-bromo-3-chlorobenzoate

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 6344Dichloromethane溶媒

実験手順

To a solution of 2-bromo-3-chlorobenzoic acid (7.29 mmol) in 20 mL DCM and 1 mL DMF was added 1.06 mL thionyl chloride. After stirring at RT overnight, 5 mL MeOH were added and stirring was continued at RT for 1 h. The reaction mixture was cooled in an ice bath, quenched by adding a sat. aq. NaHCO3 solution and extracted twice with DCM. The combined organic layers were dried over MgSO4 and concentrated in vacuo to give the desired product as colorless oil.

後処理

  1. stirringstirring
  2. waitwas continued at RT for 1 h
  3. temperatureThe reaction mixture was cooled in an ice bath
  4. customquenched
  5. additionby adding a sat. aq. NaHCO3 solution
  6. extractionextracted twice with DCM
  7. dry with materialThe combined organic layers were dried over MgSO4
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-7abd6da93a9942c59eeb9ef8012602fc
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409917B2

反応ノート

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