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Sodium Bicarbonate → HCID 23468751, 화합물

HRID 128215
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HRID 128215 반응식
[CH:1]([OH:3])=O.C(OC(=O)C)(=O)C.[F:11][C:12]([F:26])([F:25])[C:13]1[CH:14]=[C:15]([CH:19]2[CH2:24][CH2:23][CH2:22][NH:21][CH2:20]2)[CH:16]=[CH:17][CH:18]=1.C(=O)(O)[O-].[Na+]>C1C=CC=CC=1>[F:26][C:12]([F:11])([F:25])[C:13]1[CH:14]=[C:15]([CH:19]2[CH2:24][CH2:23][CH2:22][N:21]([CH:1]=[O:3])[CH2:20]2)[CH:16]=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 516892Sodium BicarbonateHCID 30490313-[3-(Trifluoromethyl)phenyl]piperidineHCID 19869020Acetic anhydride formic acid

생성물 1

HCID 23468751HCID 23468751, 화합물수율 151.5%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

3.8 g of mixed formic acid-acetic acid anhydride were added to a solution of 9.8 g of 3-(m-trifluoromethylphenyl)-piperidine in 100 ml of anhydrous benzene and the mixture was stirred for 15 minutes at room temperature and was then poured into 100 ml of aqueous sodium bicarbonate. The mixture was extracted with ethyl acetate and the organic extracts were washed with aqueous sodium chloride, dried over magnesium sulfate and evaporated to dryness to obtain 10 g of 3-(m-trifluoromethylphenyl)-1-piperidine-carboxaldehyde in the form of a colorless resin which was used as is for the next step.

후처리

  1. extractionThe mixture was extracted with ethyl acetate
  2. washthe organic extracts were washed with aqueous sodium chloride
  3. dry with materialdried over magnesium sulfate
  4. customevaporated to dryness

출처 및 근거

ORD 기록
ord-1b204679d6444f24b3caab86f4bda63f
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04259337

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