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Methane, dichloromethoxy- → 5-Bromo-1-benzothiophene-3-carbaldehyde

HRID 2061905
ノート
印刷プレビュー

反応式

HRID 2061905 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[CH:7][C:6]=2[CH:10]=1.[CH3:11][O:12]C(Cl)Cl.C([O-])(O)=O.[Na+]>ClCCCl.[Ti](Cl)(Cl)(Cl)Cl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[C:7]([CH:11]=[O:12])[C:6]=2[CH:10]=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 3

HCID 21004Methane, dichloromethoxy-HCID 516892Sodium BicarbonateHCID 27765785-Bromo-1-benzothiophene

生成物 1

HCID 75374995-Bromo-1-benzothiophene-3-carbaldehyde収率 72.9%

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒HCID 111,2-Dichloroethane
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. extractionwas extracted with DCM (2×100 mL)
  2. concentrationThe extracts were concentrated
  3. customchromatographed (0 to 5% ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-09ba93cdb6484e54aa7d503ff3be9d13
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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