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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Bentazon → Bentazone ammonium

HRID 482303
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HRID 482303 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].O.[NH3:18]>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].[NH4+:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2328BentazonHCID 12896473Azane;hydrate

생성물 1

HCID 131720800Bentazone ammonium수율 45.7%

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 stirring at 50°-60° C. with 34 g of ammonia water (5% strength solution of ammonia in water). After addition was complete, the aqueous phase was separated off at 50°-60° C. On cooling the aqueous phase, the bentazone-ammonium was deposited in crystalline form. The solid was separated off at 20° C. by filtration and freed from solvent residues under reduced pressure and at 50° C. 11.8 g of bentazone-ammonium (m.p. 180° C.) were obtained. By evaporating the water from the mother liquor under reduced pressure and at 50°-60° C., a further 13.7 g of bentazone-ammonium were obtained.

후처리

  1. additionAfter addition
  2. customthe aqueous phase was separated off at 50°-60° C
  3. temperatureOn cooling the aqueous phase
  4. customThe solid was separated off at 20° C. by filtration
  5. customfreed from solvent residues under reduced pressure and at 50° C

출처 및 근거

ORD 기록
ord-46d50470d3c3400fa5fbd4aa28670455
출처 데이터셋
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05795983

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