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Water → 2,3,5-Triiodobenzyl mesylate

HRID 58354
ノート
印刷プレビュー

反応式

HRID 58354 の反応式
[S:1](Cl)([CH3:4])(=[O:3])=[O:2].[I:6][C:7]1[C:14]([I:15])=[CH:13][C:12]([I:16])=[CH:11][C:8]=1[CH2:9][OH:10].C(N(C(C)C)CC)(C)C.O>ClCCl>[S:1]([O:10][CH2:9][C:8]1[CH:11]=[C:12]([I:16])[CH:13]=[C:14]([I:15])[C:7]=1[I:6])(=[O:3])(=[O:2])[CH3:4]
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 4

HCID 962WaterHCID 31297Methanesulfonyl chlorideHCID 81531DiisopropylethylamineHCID 34957432,3,5-Triiodobenzyl alcohol

生成物 1

HCID 866822052,3,5-Triiodobenzyl mesylate収率 84%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

Mesyl chloride (0.6 ml, 8 mmol) was added dropwise to a suspension of 2,3,5-triiodobenzyl alcohol 1 (1.94 g, 4 mmol) in dry dichloromethane (30 ml) containing diisopropylethylamine (1.4 ml, 8 mmol) at 0° C. under dry nitrogen gas flow. The reaction mixture was stirred 1 h15 at 0° C., then cold H2O (40 ml) was added. The resulting aqueous phase was extracted with dichloromethane (10 ml). The combined organic extracts were washed with H2O (8 ml) then dried (Na2SO4), filtered and concentrated. The pale yellow solid was also washed with cold methanol (35 ml). 1.894 g of 2,3,5-triiodobenzyl mesylate in the form of a white clean solid was obtained in 84% yield.

後処理

  1. extractionThe resulting aqueous phase was extracted with dichloromethane (10 ml)
  2. washThe combined organic extracts were washed with H2O (8 ml)
  3. dry with materialthen dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. washThe pale yellow solid was also washed with cold methanol (35 ml)

出典と根拠

ORDレコード
ord-06f0003fb7f04460a0642a8020f29f7e
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09434800B2

反応ノート

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