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Formic Acid → HCID 17816453、化合物

HRID 2249698
ノート
印刷プレビュー

反応式

HRID 2249698 の反応式
Br[C:2]1[C:10]2[N:9]([CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14])[C:8](=[O:16])[N:7]([CH2:17][CH2:18][CH:19]([CH3:21])[CH3:20])[C:6]=2[CH:5]=[C:4](Br)[C:3]=1[C:23]([O:25][CH3:26])=[O:24].C(O)=O.C(N(CC)CC)C.Cl>CN(C)C=O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O.C(OCC)(=O)C>[CH2:17]([N:7]1[C:6]2[CH:5]=[CH:4][C:3]([C:23]([O:25][CH3:26])=[O:24])=[CH:2][C:10]=2[N:9]([CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14])[C:8]1=[O:16])[CH2:18][CH:19]([CH3:21])[CH3:20]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 284Formic AcidHCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 17816478HCID 17816478、化合物

生成物 1

HCID 17816453HCID 17816453、化合物収率 77.9%

試薬・触媒・溶媒 4

HCID 178418397HCID 178418397、化合物
触媒
HCID 962Water溶媒
HCID 6228Dimethylformamide溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
100 °C

実験手順

In 7 ml of N,N-dimethylformamide are suspended 0.70 g of methyl 4,6-dibromo-1,3-diisopentyl-2-oxo-2,3-dihydro-1H-benzimidazole-5-carboxylate, 0.16 g of tetrakis(triphenylphosphine)palladium(0), 0.44 ml of formic acid and 2.4 ml of triethylamine. The suspension is stirred at 100° C. for 3 hours. The reaction mixture is added to a mixture of ethyl acetate and water, pH is adjusted to 4 with 2 mol/L hydrochloric acid, and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and then the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography (eluent; hexane:ethyl acetate=5:1) to obtain 0.37 g of methyl 1,3-diisopentyl-2-oxo-2,3-dihydro-1H-benzimidazole-5-carboxylate as a colorless oily product.

後処理

  1. customthe organic layer is separated
  2. customThe organic layer thus obtained
  3. washis washed with water and saturated aqueous solution of sodium chloride successively
  4. dry with materialdried over anhydrous magnesium sulfate
  5. distillationthe solvent is distilled off under reduced pressure
  6. customThe residue thus obtained
  7. customis purified by silica gel column chromatography (eluent; hexane:ethyl acetate=5:1)

出典と根拠

ORDレコード
ord-74901506a3a0406d9f6e947b3bde71a6
出典データセット
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07314888B1

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート