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Formaldehyde → HCID 69152202, 화합물

HRID 2375351
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HRID 2375351 반응식
[C:1]([C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][NH:17][C:18](=[O:20])[CH3:19])=[CH:11][CH:10]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(=O)(=O)(O)O.[CH2:26]=O>C(O)(=O)C>[C:18]([N:17]1[CH2:16][CH2:15][C:12]2[C:11](=[CH:10][C:9]([C:1]([C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[O:8])=[CH:14][CH:13]=2)[CH2:26]1)(=[O:20])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 712FormaldehydeHCID 1118Sulfuric AcidHCID 22445845HCID 22445845, 화합물

생성물 1

HCID 69152202HCID 69152202, 화합물수율 34.8%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

N-[2-(4-Benzoylphenyl)ethyl]acetamide (16.46 mmol, 4.40 g) was introduced into glacial acetic acid (20 ml). Concentrated sulfuric acid (25 ml) and then formalin (49.29 mmol, 4.00 g) were slowly added thereto at 30° C. The mixture was stirred for 2 days and poured into ice-water, and the aqueous phase was extracted with ethyl acetate. The organic phase was washed with aqueous sodium carbonate solution, dried and concentrated. The residue was stirred with diethyl ether and the solid resulting therefrom was filtered off with suction. 1.6 g of the title compound were obtained as a beige-colored solid with a melting point of 110-113° C.

후처리

  1. customat 30° C
  2. extractionthe aqueous phase was extracted with ethyl acetate
  3. washThe organic phase was washed with aqueous sodium carbonate solution
  4. customdried
  5. concentrationconcentrated
  6. stirringThe residue was stirred with diethyl ether
  7. customthe solid resulting
  8. filtrationtherefrom was filtered off with suction

출처 및 근거

ORD 기록
ord-77f4301a5a4a4350bd680a09f31053cb
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07465744B2

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