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Thionyl Chloride → 2-iodo-3-methyl-benzoyl Chloride

HRID 2216042
ノート
印刷プレビュー

反応式

HRID 2216042 の反応式
[I:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:14])=O>C1COCC1>[I:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([Cl:14])=[O:5]
参加物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 24386Thionyl ChlorideHCID 27593652-Iodo-3-methylbenzoic acid

生成物 1

HCID 110332772-iodo-3-methyl-benzoyl Chloride

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

2-iodo-3-methyl benzoic acid (1310 mg, 5 mmol) and thionyl chloride (730 μL, 10 mmol) were dissolved into THF (10 mL) and stirred at RT for 4 days. The solvents were removed in vacuo and the resulting residue was dissolved into EtOAc, washed with brine. The combined organic layers were dried (MgSO4) and the solvents were removed in vacuo resulting in an oil that was used without further purification or characterization.

後処理

  1. customThe solvents were removed in vacuo
  2. dissolutionthe resulting residue was dissolved into EtOAc
  3. washwashed with brine
  4. dry with materialThe combined organic layers were dried (MgSO4)
  5. customthe solvents were removed in vacuo
  6. customresulting in an oil that
  7. customwas used without further purification or characterization

出典と根拠

ORDレコード
ord-d81b5b181fab4c0aab92d6729fc4073b
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07109354B2

反応ノート

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