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Acetonitrile → methyl 5,6-dimethoxy-1H-indene-2-carboxylate

HRID 2175693
ノート
印刷プレビュー

反応式

HRID 2175693 の反応式
I[C:2]1[CH:9]=[C:8]([O:10][CH3:11])[C:7]([O:12][CH3:13])=[CH:6][C:3]=1[CH:4]=O.CCN(CCOC1C=CC(CC2C=CC=CC=2)=CC=1)CC.Cl.C(#N)C.[C:39]([O:43][CH3:44])(=[O:42])[CH:40]=[CH2:41]>[Zn].O>[CH3:13][O:12][C:7]1[CH:6]=[C:3]2[C:2](=[CH:9][C:8]=1[O:10][CH3:11])[CH2:41][C:40]([C:39]([O:43][CH3:44])=[O:42])=[CH:4]2
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

7

反応物 4

HCID 6342AcetonitrileHCID 7294Methyl AcrylateHCID 175534Tesmilifene HydrochlorideHCID 110117632-Iodo-4,5-dimethoxybenzaldehyde

生成物 1

HCID 12423472methyl 5,6-dimethoxy-1H-indene-2-carboxylate収率 21.3%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒
HCID 962Water溶媒

反応条件

温度
80 °C

実験手順

2-Iodo-4,5-dimethoxybenzaldehyde (292 mg, 1.0 mmol), CoCl2 (dppe) complex (26.4 mg, 0.05 mmol), dppe (19.9 mg, 0.05 mmol) and zinc power (179.8 mg, 2.75 mmol) were placed in a vial, which was sealed with a septum and flushed several times with nitrogen. Acetonitrile (3 mL) and methyl acrylate (172 mg, 2.0 mmol) were then sequentially added and the mixture was heated at 80° C. overnight. Water was then added and the mixture was extracted with ethyl acetate. The organic extracts were concentrated under reduced pressure and the residue was purified by flash chromatography using petroleum ether/ethyl acetate 8:1 (v:v) as eluent to give methyl 5,6-dimethoxy-1H-indene-2-carboxylate (50 mg, 21%). LC-MS (ES-API); rt 7.89 min; m/z calculated for C13H14O4 [M+H]+ 235.1, found 235.1.

後処理

  1. customwas sealed with a septum
  2. customflushed several times with nitrogen
  3. extractionthe mixture was extracted with ethyl acetate
  4. concentrationThe organic extracts were concentrated under reduced pressure
  5. customthe residue was purified by flash chromatography

出典と根拠

ORDレコード
ord-14bd130193fc4188902ee66da0fcd1c8
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09062076B2

反応ノート

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