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Sodium Hydroxide → HCID 19848366, 화합물

HRID 2296499
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HRID 2296499 반응식
C[O:2][C:3](=[O:17])[CH2:4][O:5][C:6]1[C:11]([Cl:12])=[CH:10][C:9]([Cl:13])=[C:8]([C:14]#[N:15])[C:7]=1[Cl:16].[OH-:18].[Na+]>O>[C:14]([C:8]1[C:7]([Cl:16])=[C:6]([C:11]([Cl:12])=[CH:10][C:9]=1[Cl:13])[O:5][CH2:4][C:3]([OH:2])=[O:17])(=[O:18])[NH2:15]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 54416269HCID 54416269, 화합물

생성물 1

HCID 19848366HCID 19848366, 화합물수율 85%

시약·촉매·용매 1

HCID 962Water용매

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온도
60 °C

실험 절차

29.4 g (0.1 mol) of 3-cyano-2,4,6-trichlorophenoxyacetic acid methyl ester are suspended in 300 ml of water. After addition of 35 ml of concentrated sodium hydroxide, the reaction mixture is heated at 60° C. until a clear solution is obtained. After filtration over active carbon, the solution is cooled and brought to pH 2 by dropwise addition of 50% concentrated hydrochloric acid. The mixture is stirred for 2 hours in an ice bath, after which the resultant precipitate is vacuum-filtered, washed with water and dried at 50° C., thus producing 25.4 g (85% of theory) of 3-carbamoyl-2,4,6-trichlorophenoxyacetic acid as a white powder, mp 261°-262° C.

후처리

  1. customis obtained
  2. filtrationAfter filtration over active carbon
  3. temperaturethe solution is cooled
  4. additionbrought to pH 2 by dropwise addition of 50% concentrated hydrochloric acid
  5. filtrationafter which the resultant precipitate is vacuum-filtered
  6. washwashed with water
  7. customdried at 50° C.

출처 및 근거

ORD 기록
ord-7a45c010618d45338f957cdf2f330558
출처 데이터셋
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04429152

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