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2,4-Dimethylthiazole → 5-(2-Methoxy-4-nitro-phenyl)-2,4-dimethyl-thiazole

HRID 2076130
ノート
印刷プレビュー

反応式

HRID 2076130 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[O:11][CH3:12].C([O-])(=O)C.[K+].[CH3:18][C:19]1[S:20][CH:21]=[C:22]([CH3:24])[N:23]=1>CN(C)C(=O)C.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:12][O:11][C:3]1[CH:4]=[C:5]([N+:8]([O-:10])=[O:9])[CH:6]=[CH:7][C:2]=1[C:21]1[S:20][C:19]([CH3:18])=[N:23][C:22]=1[CH3:24]
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 109342,4-DimethylthiazoleHCID 1012932-Bromo-5-nitroanisoleHCID 517044Potassium Acetate

生成物 1

HCID 670961295-(2-Methoxy-4-nitro-phenyl)-2,4-dimethyl-thiazole収率 62.1%

試薬・触媒・溶媒 2

HCID 11979704Tetrakis(triphenylphosphine)palladium触媒
HCID 31374
Dimethylacetamide
溶媒

実験手順

In a microwave vial a mixture of 2-bromo-5-nitroanisole (600 mg, 2.53 mmol), potassium acetate (377 mg, 3.80 mmol) and tetrakis(triphenylphosphine)-palladium(0) (148 mg, 0.13 mmol) in N,N-dimethylacetamide (8 mL) was flushed with nitrogene while 2,4-dimethylthiazole (1.47 g, 12.7 mmol) was added. The tube was sealed and the mixture irradiated for 30 minutes at 170° C. The red-brown mixture was partitioned between ethyl acetate and water. The aqueous layer was re-extracted with ethyl acetate. The combined organic phases were washed with water, with brine, dried with magnesium sulfate and the solvent was evaporated to dryness. Column chromatography (40 g silica, heptane/ethyl acetate 7:3 v/v) afforded the title compound (415 mg, 62%) as a yellow solid. MS ISP (m/e): 265.1 (100) [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.90 (dd, 1H), 7.81 (d, 1H), 7.45 (d, 1H), 3.95 (s, 3H), 2.71 (s, 3H), 2.35 (s, 3H). mp 123-125° C.

後処理

  1. additionwas added
  2. customThe tube was sealed
  3. customthe mixture irradiated for 30 minutes at 170° C
  4. customThe red-brown mixture was partitioned between ethyl acetate and water
  5. extractionThe aqueous layer was re-extracted with ethyl acetate
  6. washThe combined organic phases were washed with water, with brine
  7. dry with materialdried with magnesium sulfate
  8. customthe solvent was evaporated to dryness

出典と根拠

ORDレコード
ord-17767fb3db9b407ca09ec20f44737c7b
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07923450B2

反応ノート

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