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Triethylamine → HCID 117761061、化合物

HRID 1748420
ノート
印刷プレビュー

反応式

HRID 1748420 の反応式
Br[CH2:2][C:3]1[CH:8]=[C:7]([Br:9])[CH:6]=[C:5]([Br:10])[C:4]=1[OH:11].N[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[SH:19].C([N:22](CC)CC)C>C1COCC1>[NH2:22][S:19][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[CH2:2][C:3]1[CH:8]=[C:7]([Br:9])[CH:6]=[C:5]([Br:10])[C:4]=1[OH:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 87132-AminothiophenolHCID 6221772,4-Dibromo-6-(bromomethyl)phenol

生成物 1

HCID 117761061HCID 117761061、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 2-(bromomethyl)-4,6-dibromophenol (1.48 g, 4.3 mmol) in THF (20 mL) was added dropwise to a solution of 2-Aminothiophenol (0.54 g, 4.3 mmol) and triethylamine (0.60 mL) in THF (20 mL) and stirred at room temperature for 12 hours. A solid had formed and was filtered out followed by removal of the solvent in vacuum. The crude product was dissolved in dichloromethane, washed with saturated NaCl solution and dried over MgSO4. The product was obtained as a yellow oil in a quantitative yield.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customA solid had formed
  2. filtrationwas filtered out
  3. customfollowed by removal of the solvent in vacuum
  4. dissolutionThe crude product was dissolved in dichloromethane
  5. washwashed with saturated NaCl solution
  6. dry with materialdried over MgSO4
  7. customThe product was obtained as a yellow oil in a quantitative yield

出典と根拠

ORDレコード
ord-fd9e5684b8d14df18d4376d0db64dd4d
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09150676B2

反応ノート

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