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Water → HCID 11666911、化合物

HRID 2061906
ノート
印刷プレビュー

反応式

HRID 2061906 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[C:7]([CH:10]=O)[C:6]=2[CH:12]=1.[S:13]([NH2:17])([NH2:16])(=[O:15])=[O:14].[BH4-].[Na+].O>C(O)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[C:7]([CH2:10][NH:16][S:13]([NH2:17])(=[O:15])=[O:14])[C:6]=2[CH:12]=1
参加物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 82267SulfamideHCID 4311764Sodium borohydrideHCID 75374995-Bromo-1-benzothiophene-3-carbaldehyde

生成物 1

HCID 11666911HCID 11666911、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

5-Bromobenzothiophene (1.60 g, 7.51 mmol) and dichloromethyl methyl ether (1.29 g, 11.3 mmol) were dissolved in anhydrous 1,2-dichloroethane (75 mL). Titanium tetrachloride (2.14 g, 11.3 mmol) was added, turning the solution dark. After one hour at room temperature, the reaction was poured into a mixture of saturated aqueous NaHCO3 and ice. The mixture was stirred for about 30 minutes and then was extracted with DCM (2×100 mL). The extracts were concentrated and chromatographed (0 to 5% ethyl acetate in hexane) to yield 5-bromo-benzo[b]thiophene-3-carbaldehyde (1.32 g). The 5-bromobenzothiophene-3-carboxaldehyde (1.20 g, 4.98 mmol) and sulfamide (4.0 g, 42 mmol) were combined in anhydrous ethanol (25 mL) and heated to reflux for three days. The reaction was cooled to room temperature and sodium borohydride (0.207 g, 5.47 mmol) was added. After five hours, water (50 ml) was added and the solution was extracted with chloroform (3×50 mL). The extracts were concentrated, suspended in a minimal amount of DCM, and filtered to provide the title compound as a yellow solid.

後処理

  1. temperatureheated
  2. temperatureto reflux for three days
  3. extractionthe solution was extracted with chloroform (3×50 mL)
  4. concentrationThe extracts were concentrated
  5. filtrationfiltered

出典と根拠

ORDレコード
ord-829ead83669e472299de5963e22d9e6a
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08283478B2

反応ノート

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