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Hydrochloric Acid → 1-(2-Hydroxyethyl)-2-imidazolinethione

HRID 256540
ノート
印刷プレビュー

反応式

HRID 256540 の反応式
OC[CH2:3][NH:4][CH2:5][CH2:6][NH2:7].C(=S)=[S:9].Cl.[CH2:12]([OH:14])[CH3:13].O>>[OH:14][CH2:12][CH2:13][N:4]1[CH2:5][C:6](=[S:9])[N:7]=[CH:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 313Hydrochloric AcidHCID 6348Carbon Disulfide3 回HCID 8112N-(2-Hydroxyethyl)ethylenediamineHCID 19096565Water ethanol

生成物 1

HCID 197853781-(2-Hydroxyethyl)-2-imidazolinethione

実験手順

(Hydroxyethyl)ethylenediamine (25 ml) is dissolved in 1:1 ethyl alcohol-water (85 mL) and heated to 40°-50° C. Carbon disulfide (16.5 ml) is added dropwise over a period of about 15 minutes. After about half of the amount is added, the exothermic reaction starts and the reaction mixture solidifies. After the addition of all of the carbon disulfide, the mixture is refluxed gently for about 1 hour. Concentrated hydrochloric acid (2 ml) is then added and the reaction mixture is refluxed overnight. The solid which separates after the addition of carbon disulfide redissolves. The solution is cooled in an ice bath, and the solid separates, is filtered out, washed well with isopropyl alcohol and t-butyl methyl ether and dried to give 23.3 g of 1-(2-hydroxyethyl)-2-imidazolinethione, melting point 137°-138° C.

後処理

  1. temperatureheated to 40°-50° C
  2. additionAfter about half of the amount is added
  3. customthe exothermic reaction starts
  4. temperaturethe mixture is refluxed gently for about 1 hour
  5. temperaturethe reaction mixture is refluxed overnight
  6. dissolutionredissolves
  7. temperatureThe solution is cooled in an ice bath
  8. filtrationthe solid separates, is filtered out
  9. washwashed well with isopropyl alcohol and t-butyl methyl ether
  10. customdried

出典と根拠

ORDレコード
ord-eedbe9a592fe4d859221132b42e65042
出典データセット
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05258381

反応ノート

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