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Methyl chloroformate → Methyl 2,3-dihydro-1H-indole-1-carboxylate

HRID 965544
ノート
印刷プレビュー

反応式

HRID 965544 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.Cl[C:11]([O:13][CH3:14])=[O:12]>N1C=CC=CC=1.C(Cl)Cl>[CH3:14][O:13][C:11]([N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1)=[O:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 6586Methyl chloroformate2 回HCID 10328Indoline

生成物 1

HCID 690083Methyl 2,3-dihydro-1H-indole-1-carboxylate収率 56%

試薬・触媒・溶媒 2

HCID 1049Pyridine溶媒HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of 10 g of indoline in 10 ml of pyridine is cooled to 0° C. a solution of 7.9 g of methyl chloroformate in 10 ml of DCM is added dropwise and the mixture is stirred for 1 hour at 0C. A further solution of 7.9 g of methyl chloroformate in 10 ml of DCM is then added and the reaction mixture is concentrated under vacuum. The residue is taken up with water and extracted with AcOEt, the organic phase is washed with a 5% solution of potassium hydrogensulfate, with water and with a saturated solution of NaCl and dried over sodium sulfate and the solvent is evaporated off under vacuum to give 8.3 g of the expected product after trituration in a DCM/iso ether mixture and then filtration. M.p.=69°-70° C.

後処理

  1. additionis added dropwise
  2. concentrationthe reaction mixture is concentrated under vacuum
  3. extractionextracted with AcOEt
  4. washthe organic phase is washed with a 5% solution of potassium hydrogensulfate, with water and with a saturated solution of NaCl
  5. dry with materialdried over sodium sulfate
  6. customthe solvent is evaporated off under vacuum

出典と根拠

ORDレコード
ord-c127e19238534cd3b50943ffc8b677e8
出典データセット
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05773612

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート