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Triethylamine → 5,5-Dimethyl-3-{4-[(trifluoromethyl)sulfanyl]phenyl}imidazolidine-2,4-dione

HRID 1169670
ノート
印刷プレビュー

反応式

HRID 1169670 の反応式
C(N(CC)CC)C.Cl.[NH2:9][C:10]([CH3:16])([CH3:15])[C:11](OC)=[O:12].[F:17][C:18]([S:21][C:22]1[CH:27]=[CH:26][C:25]([N:28]=[C:29]=[O:30])=[CH:24][CH:23]=1)([F:20])[F:19]>C1(C)C=CC=CC=1.C(OCC)C>[CH3:16][C:10]1([CH3:15])[NH:9][C:29](=[O:30])[N:28]([C:25]2[CH:24]=[CH:23][C:22]([S:21][C:18]([F:20])([F:17])[F:19])=[CH:27][CH:26]=2)[C:11]1=[O:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 8471TriethylamineHCID 27333921-Isocyanato-4-[(trifluoromethyl)sulfanyl]benzeneHCID 13258034Methyl 2-aminoisobutyrate hydrochloride

生成物 1

HCID 132680685,5-Dimethyl-3-{4-[(trifluoromethyl)sulfanyl]phenyl}imidazolidine-2,4-dione収率 95.6%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒
HCID 3283
Diethyl Ether
溶媒

反応条件

温度
20 °C

実験手順

5.12 ml of triethylamine and 2.8 g of methyl α-aminoisobutyrate hydrochloride are added to a solution of 4 g of 4-trifluoromethylsulfanylphenyl isocyanate in 40 ml of toluene, under an inert atmosphere of argon at a temperature in the region of 20° C. The mixture thus obtained is refluxed for 24 hours and then cooled to a temperature in the region of 20° C. The reaction mixture is concentrated to dryness under reduced pressure and the residue obtained is taken up in ethyl ether and filtered. 5.3 g of 5,5-dimethyl-3-(4-trifluoromethylsulfanylphenyl)-imidazolidine-2,4-dione are thus obtained, the characteristics of which product are as follows:

後処理

  1. customThe mixture thus obtained
  2. temperatureis refluxed for 24 hours
  3. concentrationThe reaction mixture is concentrated to dryness under reduced pressure
  4. customthe residue obtained
  5. filtrationfiltered

出典と根拠

ORDレコード
ord-a0a73dd2ba1a4665b8209848a0095ba4
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07825115B2

反応ノート

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