Pyridine → Methyl 3-(5-p-tolylisoxazol-3-yl)benzoate

HRID 2113907ノート

反応式

HRID 2113907 の反応式
[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10](Cl)=[N:11][OH:12])[CH:5]=1.[C:15]([C:17]1[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=1)#[CH:16].N1C=CC=CC=1.C(N(CC)CC)C>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]2[CH:16]=[C:15]([C:17]3[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=3)[O:12][N:11]=2)[CH:5]=1

参加物

6

反応物 4

HCID 1049PyridineHCID 8471TriethylamineHCID 13018p-EthynyltolueneHCID 85867392Methyl 3-[chloro(hydroxyimino)methyl]benzoate

生成物 1

HCID 57907091Methyl 3-(5-p-tolylisoxazol-3-yl)benzoate

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

In a 25 ml round flask, 1.9 g (8.9 mmol) of 3-[chloro-(hydroxyimino)-methyl]-benzoic acid methyl ester and 1.03 g (8.9 mmol) of 1-ethynyl-4-methyl-benzene are dissolved in 12 ml of CHCl3 at 0° C. To this solution, 36 μl (0.4 mmol, 0.05 eq.) of pyridine and subsequently 1.24 ml (8.9 mmol) of triethyl amine are added and the mixture is stirred under warming to room temperature for 2 h. Then, the mixture is poured onto water, extracted twice with CH2Cl2, the organic layers are dried with brine and Na2SO4 and then concentrated. Chromatographic purification (250 g SiO2; gradient elution, eluent: hexane/ethyl acetate 95:5→9:1) yields the title compound as a white solid. Mass spectrum: m/z (M+H)+: 294.2

後処理

  1. additionThen, the mixture is poured onto water
  2. extractionextracted twice with CH2Cl2
  3. dry with materialthe organic layers are dried with brine and Na2SO4
  4. concentrationconcentrated
  5. customChromatographic purification (250 g SiO2; gradient elution, eluent: hexane/ethyl acetate 95:5→9:1)

出典と根拠

ORDレコード
ord-6021b36f6361478ba2cfafada77afcf8
出典データセット
uspto-grants-2008_10
特許番号
US07432293B2

反応ノート

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