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

HRID 965544
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HRID 965544 반응식
[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]
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참가 물질

5

반응물 2

HCID 6586Methyl chloroformate2회HCID 10328Indoline

생성물 1

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

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 6344Dichloromethane용매2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c127e19238534cd3b50943ffc8b677e8
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05773612

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