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Methyl chloroformate → Methyl [6-(trifluoromethyl)pyridin-3-yl]carbamate

HRID 1445468
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HRID 1445468 반응식
[F:1][C:2]([F:11])([F:10])[C:3]1[N:8]=[CH:7][C:6]([NH2:9])=[CH:5][CH:4]=1.Cl[C:13]([O:15][CH3:16])=[O:14].C(=O)(O)[O-].[Na+]>N1C=CC=CC=1>[F:11][C:2]([F:1])([F:10])[C:3]1[N:8]=[CH:7][C:6]([NH:9][C:13](=[O:14])[O:15][CH3:16])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6586Methyl chloroformateHCID 516892Sodium BicarbonateHCID 27377445-Amino-2-(trifluoromethyl)pyridine

생성물 1

HCID 23082060Methyl [6-(trifluoromethyl)pyridin-3-yl]carbamate

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Into 15 ml of pyridine was dissolved 3.00 g of 6-(trifluoromethyl)pyridin-3-amine, and then 2.1 ml of methyl chloroformate was added thereto under ice-cooling, followed by 2 hours of stirring at room temperature. Under ice-cooling, 30 ml of a saturated sodium bicarbonate aqueous solution was added to the reaction solution, followed by 1 hour of stirring. Thereafter, the precipitated crystals were filtrated and, after washing with water, dried under reduced pressure to obtain 3.88 g of the title compound.

후처리

  1. temperatureunder ice-cooling
  2. temperatureUnder ice-cooling
  3. waitfollowed by 1 hour
  4. stirringof stirring
  5. filtrationThereafter, the precipitated crystals were filtrated
  6. washafter washing with water
  7. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-4b873387533240b487857216d3fd5652
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07666873B2

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