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Diethylamine → 4-dichloromethylene-N,N-diethyl-2-trichloromethylbenzo[1,3]dioxin-6-carboxamide

HRID 224391
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HRID 224391 반응식
[Cl:1][C:2]([Cl:21])([Cl:20])[CH:3]1[O:8][CH:7]([C:9](Cl)([Cl:11])[Cl:10])[C:6]2[CH:13]=[C:14]([C:17](Cl)=[O:18])[CH:15]=[CH:16][C:5]=2[O:4]1.[CH2:22]([NH:24][CH2:25][CH3:26])[CH3:23]>>[Cl:10][C:9]([Cl:11])=[C:7]1[C:6]2[CH:13]=[C:14]([C:17]([N:24]([CH2:25][CH3:26])[CH2:22][CH3:23])=[O:18])[CH:15]=[CH:16][C:5]=2[O:4][CH:3]([C:2]([Cl:20])([Cl:21])[Cl:1])[O:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 8021DiethylamineHCID 233329602,4-Bis(trichloromethyl)-2H,4H-1,3-benzodioxine-6-carbonyl chloride

생성물 1

HCID 233329274-dichloromethylene-N,N-diethyl-2-trichloromethylbenzo[1,3]dioxin-6-carboxamide

실험 절차

A mixture of 2,4-bis(trichloromethyl)benzo[1,3]dioxin-6-carbonyl chloride (2 g.) and diethylamine (25 ml.) was heated under reflux for 2 hrs., cooled, and filtered to remove diethylamine hydrochloride. The filtrate was evaporated to dryness under reduced pressure, and the residue was crystallised from ethanol to give 4-dichloromethylene-N,N-diethyl-2-trichloromethylbenzo[1,3]dioxin-6-carboxamide, m.p. 123°-124° C.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 2 hrs
  3. temperature, cooled
  • filtrationfiltered
  • customto remove diethylamine hydrochloride
  • customThe filtrate was evaporated to dryness under reduced pressure
  • customthe residue was crystallised from ethanol
  • 출처 및 근거

    ORD 기록
    ord-79420fbaf6684c2cb28d487ece978294
    출처 데이터셋
    uspto-grants-1980_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04232032

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