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Ethyl orthoformate → HCID 22561750, 화합물

HRID 983071
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HRID 983071 반응식
C([O:8][CH2:9][CH3:10])(OCC)OCC.[CH3:11][C:12]1[NH:13][CH:14]=[C:15](C)[C:16]=1[C:17]1[CH2:18][CH2:19][N:20]([CH3:23])[CH2:21][CH:22]=1>C(O)(C(F)(F)F)=O>[CH3:14][C:15]1[C:16]([C:17]2[CH2:22][CH2:21][N:20]([CH3:23])[CH2:19][CH:18]=2)=[C:12]([CH3:11])[NH:13][C:10]=1[CH:9]=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31214Ethyl orthoformateHCID 22561850HCID 22561850, 화합물

생성물 1

HCID 22561750HCID 22561750, 화합물

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

반응 조건

온도
0 °C

실험 절차

Triethyl orthoformate (6 mL) was added to a solution of 4-(2,4-dimethyl-1H-pyrrol-3-yl)-1-methyl-1,2,3,6-tetrahydro-pyridine (360 mg) in TFA (6 mL) at 0° C. The mixture was stirred at 0° C. for 10 mins and then at rt for 40 mins. The solvent was removed and to the residue was added NaHCO3, extracted with ethyl acetate, dried and concentrated to give 356 mg of 3,5-dimethyl-4-(1-methyl-1,2,3,6-tetrahydro-pyridin-4-yl)-1H-pyrrole-2-carbaldehyde.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. waitat rt for 40 mins
  2. customThe solvent was removed and to the residue
  3. additionwas added NaHCO3
  4. extractionextracted with ethyl acetate
  5. customdried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6fd06f2538ee47749a7aa4697b16ad9c
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06861418B2

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