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Triethylamine → ethyl 3-bromo-4-chloro-5-methyl-1H-pyrrole-2-carboxylate

HRID 655752
ノート
印刷プレビュー

反応式

HRID 655752 の反応式
[Br:1]Br.[Cl:3][C:4]1[CH:5]=[C:6]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[NH:7][C:8]=1[CH3:9].CCN(CC)CC.OS([O-])=O.[Na+]>C(Cl)Cl>[Br:1][C:5]1[C:4]([Cl:3])=[C:8]([CH3:9])[NH:7][C:6]=1[C:10]([O:12][CH2:13][CH3:14])=[O:11]
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 8471TriethylamineHCID 24408BromineHCID 23665763Sodium BisulfiteHCID 66707189ethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylate

生成物 1

HCID 66707680ethyl 3-bromo-4-chloro-5-methyl-1H-pyrrole-2-carboxylate収率 106.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane
溶媒

実験手順

Bromine (0.56 ml, 11 mmol) was added to a solution of 1 g (5.3 mmol) of ethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylate (WO2006087543) and 0.8 ml (5.7 mmol) Et3N in CH2Cl2. After stirring at room temperature for 2 h, aqueous NaHSO3 was added and the CH2Cl2 was removed and the aqueous residue was partitioned between water and EtOAc. The EtOAc layer was separated and washed with brine. The EtOAc layer was dried over anhydrous MgSO4, and the solvent was removed to give 1.5 g of the product as a solid. MS (ES) (MH+): 240 for C8H9BrClNO2; NMR (d6-DMSO): 1.3 (t, 3H), 2.2 (s, 3H), 4.2 (q, 2H), 12.3 (s, 1H).

後処理

  1. customthe CH2Cl2 was removed
  2. customthe aqueous residue was partitioned between water and EtOAc
  3. customThe EtOAc layer was separated
  4. washwashed with brine
  5. dry with materialThe EtOAc layer was dried over anhydrous MgSO4
  6. customthe solvent was removed

出典と根拠

ORDレコード
ord-f8c919a1364e42e788a071f2188cd9ef
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08071605B2

反応ノート

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