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Dimethylformamide → Ethyl 4-azido-2,6-bis(trifluoromethyl)-3-pyridinecarboxylate

HRID 542121
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HRID 542121 반응식
[F:1][C:2]([F:20])([F:19])[C:3]1[C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[C:7](Cl)[CH:6]=[C:5]([C:15]([F:18])([F:17])[F:16])[N:4]=1.[N-:21]=[N+:22]=[N-:23].[Na+].CN(C=O)C>O>[N:21]([C:7]1[CH:6]=[C:5]([C:15]([F:18])([F:17])[F:16])[N:4]=[C:3]([C:2]([F:20])([F:19])[F:1])[C:8]=1[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[N+:22]=[N-:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 33557Sodium AzideHCID 138828774-Chloro-2,6-bis-trifluoromethyl-nicotinic acid ethyl ester

생성물 1

HCID 13882885Ethyl 4-azido-2,6-bis(trifluoromethyl)-3-pyridinecarboxylate수율 83.1%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 5.0 g (0.0155 mol) of product of Example 19, 1.0 g (0.0154 mol) of sodium azide and 20 ml of DMF was stirred for 1 hour and poured into 100 ml of water. The organic was extracted into 100 ml of CH2Cl2 which was washed with 50 ml of water and concentrated. The residue (6.0 g) was dissolved in 50 ml of petroleum ether then washed with 50 ml of water twice, dried (MgSO4) and concentrated to give a solid which was recrystallized from petroluem ether at low temperature to give 4.2 g (82%) of product as a light yellow solid; mp 63°-64.5° C.

후처리

  1. extractionThe organic was extracted into 100 ml of CH2Cl2 which
  2. washwas washed with 50 ml of water
  3. concentrationconcentrated
  4. dissolutionThe residue (6.0 g) was dissolved in 50 ml of petroleum ether
  5. washthen washed with 50 ml of water twice
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated
  8. customto give a solid which
  9. customwas recrystallized from petroluem ether at low temperature

출처 및 근거

ORD 기록
ord-8564da8a4658472083faeaf0f75aaad7
출처 데이터셋
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04655816

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