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Iodine → 2-[{2-(1,3-Benzodioxol-5-yl)ethyl}dithio]ethanol

HRID 486930
ノート
印刷プレビュー

反応式

HRID 486930 の反応式
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH2:11][SH:12])=[CH:9][C:4]=2[O:3][CH2:2]1.[SH:13][CH2:14][CH2:15][OH:16].II.C(OCC)(=O)C>C(O)C.O>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH2:11][S:12][S:13][CH2:14][CH2:15][OH:16])=[CH:9][C:4]=2[O:3][CH2:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 807IodineHCID 15672-MercaptoethanolHCID 8857Ethyl AcetateHCID 158195122-(1,3-Benzodioxol-5-yl)ethanethiol

生成物 1

HCID 190016232-[{2-(1,3-Benzodioxol-5-yl)ethyl}dithio]ethanol収率 23.2%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
HCID 962
Water
溶媒

実験手順

35 g of 2-(1,3-benzodioxol-5-yl)ethanethiol and 75 g of 2-mercaptoethanol were dissolved in 150 ml of ethanol, followed by the addition of 43 g of iodine. The obtained mixture was stirred at a room temperature for 30 minutes, followed by the addition of 2 l of ethyl acetate and 2 l of water. The mixture was separated into two phases. The ethyl acetate layer was washed with water twice, then with 1 l of a 1% aqueous solution of sodium hydrogensulfite twice and finally with water thrice, dried over anhydrous sodium sulfate and filtered. The filtrate was distilled to remove the solvent. The residue was purified by silica gel column chromatography (benzen/ethyl acetate=10:1) to obtain 11.5 g of the title compound as a colorless oil.

後処理

  1. customThe mixture was separated into two phases
  2. washThe ethyl acetate layer was washed with water twice
  3. dry with materialwith 1 l of a 1% aqueous solution of sodium hydrogensulfite twice and finally with water thrice, dried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. distillationThe filtrate was distilled
  6. customto remove the solvent
  7. customThe residue was purified by silica gel column chromatography (benzen/ethyl acetate=10:1)

出典と根拠

ORDレコード
ord-eac26d4d03844644ae908bfaea7ff619
出典データセット
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05292901

反応ノート

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