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Methyl chloroformate → Methyl 2-(4-cyanonaphthalen-1-yl)acetate

HRID 132689
ノート
印刷プレビュー

反応式

HRID 132689 の反応式
[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([C:12]#[N:13])=[CH:4][CH:3]=1.[Li+].CC([N-]C(C)C)C.Cl[C:23]([O:25][CH3:26])=[O:24]>C1COCC1>[CH3:26][O:25][C:23](=[O:24])[CH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([C:12]#[N:13])=[CH:4][CH:3]=1
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

5

反応物 3

HCID 6586Methyl chloroformateHCID 1420471-Cyano-4-methylnaphthaleneHCID 2724682Lithium diisopropylamide

生成物 1

HCID 59734598Methyl 2-(4-cyanonaphthalen-1-yl)acetate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

To a solution of 4-methyl-1-cyanonaphthalene (4.35 g, 25.9 mmol) in THF (100 mL) was cooled to −78° C. and treated with commercially available LDA (2 M, 60 mL). The reaction mixture was then warmed to 0° C. and maintained at 0° C. for 30 min. The resulting red-colored solution was cooled to −78° C. and methyl chloroformate (10 mL, 130 mmol) was added. The reaction mixture was stirred while warming to rt until the displacement was complete (4 h) and then quenched with sat'd NH4Cl. The THF layer was evaporated and extracted with EtOAc (3×20 mL). The EtOAc was dried over Na2SO4 and concentrated in vacuo to afford an oil.

後処理

  1. temperaturemaintained at 0° C. for 30 min
  2. temperatureThe resulting red-colored solution was cooled to −78° C.
  3. temperaturewhile warming to rt until the displacement
  4. custom(4 h)
  5. customquenched with sat'd NH4Cl
  6. customThe THF layer was evaporated
  7. extractionextracted with EtOAc (3×20 mL)
  8. dry with materialThe EtOAc was dried over Na2SO4
  9. concentrationconcentrated in vacuo
  10. customto afford an oil

出典と根拠

ORDレコード
ord-fcac02bdec0b40e194a5e595e8dc174e
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07388027B2

反応ノート

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