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Dimethylamine → Bentazone dimethylammonium

HRID 482304
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반응식

HRID 482304 반응식
[CH3:1][CH:2]([N:4]1[S:14](=[O:16])(=[O:15])[NH:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:5]1=[O:6])[CH3:3].[CH3:17][NH:18][CH3:19]>ClCCCl>[CH3:3][CH:2]([N:4]1[S:14](=[O:16])(=[O:15])[NH:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:5]1=[O:6])[CH3:1].[CH3:17][NH2+:18][CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 674DimethylamineHCID 2328Bentazon

생성물 1

HCID 131720801Bentazone dimethylammonium

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

A solution of 24 g of bentazone (IIa) in 216 g of 1,2-dichloroethane was treated with 22.5 g of a 20% strength aqueous solution of dimethylamine with stirring at 30°-50° C. After addition was complete, the aqueous phase was separated off at 50°-60° C. and evaporated to dryness under reduced pressure and at 50°-60° C. 28 g of bentazone-dimethylammonium (m.p. 145°-147° C.; purity >99% according to HPLC analysis for bentazone and titration for dimethylammonium) were obtained.

후처리

  1. additionAfter addition
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customthe aqueous phase was separated off at 50°-60° C.
  • customevaporated to dryness under reduced pressure and at 50°-60° C
  • 출처 및 근거

    ORD 기록
    ord-b46bb2f7c7ef461e94f45d6aa06e7fa5
    출처 데이터셋
    uspto-grants-1998_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05795983

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