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Hydrochloric Acid → 2-Chloro-3-hydroxy-5-iodophenyl acetate

HRID 62762
ノート
印刷プレビュー

反応式

HRID 62762 の反応式
[C:1]([O:4][C:5]1[CH:10]=[C:9]([I:11])[CH:8]=[C:7]([O:12]C(=O)C)[C:6]=1[Cl:16])(=[O:3])[CH3:2].[OH-].[Li+].Cl>O.O1CCOCC1>[C:1]([O:4][C:5]1[CH:10]=[C:9]([I:11])[CH:8]=[C:7]([OH:12])[C:6]=1[Cl:16])(=[O:3])[CH3:2]
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

6

反応物 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 679777952-Chloro-5-iodo-1,3-phenylene diacetate

生成物 1

HCID 670418062-Chloro-3-hydroxy-5-iodophenyl acetate収率 107.7%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
60 °C

実験手順

A mixture of 2-chloro-5-iodo-1,3-phenylene diacetate (5) (5.16 g, 14.5 mmol) and 1M lithium hydroxide (29.1 mL, 29.1 mmol) in H2O (5 mL) and dioxane (20 mL) was stirred at 60° C. for 4 h then at RT for 20 h. The reaction mixture was acidified by the addition of 1M HCl and the product was extracted with EtOAc (150 mL). The organic solution was dried over MgSO4 and the solvent was removed in vacuo. The resulting oil was slurried with 1:1 DCM: isohexanes and the solvents were removed in vacuo to yield 2-chloro-3-hydroxy-5-iodophenyl acetate (6) (4.88 g, 86%) as a brown solid: m/z 311 [M−H]− (ES−).

後処理

  1. waitat RT for 20 h
  2. extractionthe product was extracted with EtOAc (150 mL)
  3. dry with materialThe organic solution was dried over MgSO4
  4. customthe solvent was removed in vacuo
  5. customisohexanes and the solvents were removed in vacuo

出典と根拠

ORDレコード
ord-edc0c41070d64205b98e788d99bcca61
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09447028B2

反応ノート

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