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N,N-Diethylethylenediamine → HCID 70549843, 화합물

HRID 2286933
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HRID 2286933 반응식
[CH2:1]([N:3]([CH2:6][CH2:7][NH2:8])[CH2:4][CH3:5])[CH3:2].[O:9]1[C:14]2[CH:15]=[CH:16][CH:17]=[C:18]([C:19]([Cl:21])=[O:20])[C:13]=2[O:12][CH2:11][CH2:10]1>CC(C)=O>[ClH:21].[CH2:1]([N:3]([CH2:6][CH2:7][NH:8][C:19]([C:18]1[C:13]2[O:12][CH2:11][CH2:10][O:9][C:14]=2[CH:15]=[CH:16][CH:17]=1)=[O:20])[CH2:4][CH3:5])[CH3:2]
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참가 물질

4

반응물 2

HCID 60993N,N-DiethylethylenediamineHCID 27950312,3-Dihydro-1,4-benzodioxine-5-carbonyl chloride

생성물 1

HCID 70549843HCID 70549843, 화합물수율 64.2%

시약·촉매·용매 1

HCID 180Acetone용매

반응 조건

온도
0 °C

실험 절차

21 g of diethylaminoethylamine and 85 ml of acetone were introduced into a balloon flask provided with an agitator and a thermometer. The mixture was cooled to 0° C. and then 36 g of 1,4-benzodioxane-5-carbonyl chloride were added. The crystals formed at ambient temperature were dried off, washed with acetone, dried and purified by recrystallization from isopropyl alcohol. 36.5 g of N-(diethylaminoethyl)-1,4-benzodioxane-5-carboxamide hydrochloride were obtained (M.P.: 120° C.; yield: 64%).

후처리

  1. customprovided with an agitator
  2. customThe crystals formed at ambient temperature
  3. customwere dried off
  4. washwashed with acetone
  5. customdried
  6. custompurified by recrystallization from isopropyl alcohol

출처 및 근거

ORD 기록
ord-b492a426c9d9433b814fd0d31c902107
출처 데이터셋
uspto-grants-1981_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04268512

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