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Hydrogen Bromide → HCID 20300309、化合物

HRID 1733118
ノート
印刷プレビュー

反応式

HRID 1733118 の反応式
C(N(CC)CC)C.[CH3:8][N:9]1[C:13](=[O:14])[C:12](=[O:15])[NH:11][C:10]1=[S:16].Br[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][Br:23].Br>CS(C)=O.CCCCCC>[Br:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][N:11]1[C:12](=[O:15])[C:13](=[O:14])[N:9]([CH3:8])[C:10]1=[S:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 260Hydrogen BromideHCID 81001,5-DibromopentaneHCID 8471TriethylamineHCID 203003261-Methyl-2-sulfanylideneimidazolidine-4,5-dione

生成物 1

HCID 20300309HCID 20300309、化合物収率 46%

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒
HCID 8058
Hexane
溶媒

実験手順

Triethylamine (84 ml, 0.60 mole) was added dropwise over a period of 6 hours to a stirred solution of 1-methyl-2-thioxo-4,5-imidazolidinedione (88 g, 0.61 mole) and 1,5-dibromopentane (264 g, 1.20 mole) in dimethylsulphoxide (650 ml) at room temperature. The mixture was allowed to stand overnight and then poured into ice water (3 liters) containing concentrated hydrobromic acid (1 ml). The mixture was extracted with chloroform and the extracts were washed with water, dried over magnesium sulphate and evaporated to give an oil which was treated with hexane to give yellow crystals of 1-(5-bromopentyl)-3-methyl-2-thioxo-4,5-imidazolidinedione (82.3 g), m.p. 48°-50°.

後処理

  1. extractionThe mixture was extracted with chloroform
  2. washthe extracts were washed with water
  3. dry with materialdried over magnesium sulphate
  4. customevaporated
  5. customto give an oil which

出典と根拠

ORDレコード
ord-2bf610db2b0442259bfac1a2bcc8e2fb
出典データセット
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USRE030457

反応ノート

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