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2,2-Diethoxyethylamine → HCID 13911324, 화합물

HRID 622189
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HRID 622189 반응식
[H][H].[CH3:3][O:4][C:5]1[C:12]2[O:13][CH2:14][O:15][C:11]=2[CH:10]=[CH:9][C:6]=1[CH:7]=O.[CH2:16]([O:18][CH:19]([O:22][CH2:23][CH3:24])[CH2:20][NH2:21])[CH3:17]>[Pt]=O.C(O)C>[CH2:16]([O:18][CH:19]([O:22][CH2:23][CH3:24])[CH2:20][NH:21][CH2:7][C:6]1[CH:9]=[CH:10][C:11]2[O:15][CH2:14][O:13][C:12]=2[C:5]=1[O:4][CH3:3])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 695242,2-DiethoxyethylamineHCID 101979461,3-Benzodioxole-5-carboxaldehyde, 4-methoxy-HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 13911324HCID 13911324, 화합물수율 100.3%

시약·촉매·용매 2

HCID 82844Platinum oxide (PtO)촉매HCID 702Ethanol
용매
2회

실험 절차

One gram of platinum oxide catalyst was added to 100 ml of ethanol, through which hydrogen was passed with stirring for 30 minutes. Then, 54.06 g (0.3 mol) of 2-methoxy-3,4-methylenedioxybenzaldehyde (1) and 40.78 g (0.3 mol) of aminoacetaldehyde diethylacetal (98 % purity) in 100 ml of ethanol were added to carry out hydrogenation with stirring at room temperature for 8.5 hours. The catalyst was filtered out and the solvent was distilled off under vacuum to obtain 89.43 g of N-(2-methoxy-3,4-methylenedioxybenzyl)aminoacetaldehyde diethylacetal (2) (yield 100 %) as an oil. IR and NMR spectra of the resultant product are listed below. ##STR20##

후처리

  1. stirringwith stirring at room temperature for 8.5 hours
  2. filtrationThe catalyst was filtered out
  3. distillationthe solvent was distilled off under vacuum

출처 및 근거

ORD 기록
ord-d586d3aa1ea747ffada5527011919678
출처 데이터셋
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04769480

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