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Hydrazine hydrate (1:1) → HCID 13531592、化合物

HRID 1660382
ノート
印刷プレビュー

反応式

HRID 1660382 の反応式
[CH3:1][O:2][CH:3]([O:8][CH3:9])[CH2:4][N:5]=[C:6]=[S:7].O.[NH2:11][NH2:12]>C(O)C>[CH3:1][O:2][CH:3]([O:8][CH3:9])[CH2:4][NH:5][C:6](=[S:7])[NH:11][NH2:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 144710Isothiocyanatoacetaldehyde dimethyl acetal

生成物 1

HCID 13531592HCID 13531592、化合物収率 70.4%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

2,2-Dimethoxyethyl isothiocyanate (37.7 g) is added in the course of 1 hour to a solution of hydrazine hydrate (14.35 g) in ethanol (40 cc), whilst stirring at a temperature of between 5° and 9° C. After 12 hours at 4° C., the mixture is concentrated to dryness at 20° C. under reduced pressure (20 mm Hg; 2.7 kPa). The yellow syrup obtained crystallises after seeding. The solid is dissolved in hot methanol (50 cc) and the solution is filtered and diluted with diethyl ether (200 cc). After about ten hours at 4° C., the mixture is filtered and 4-(2,2-dimethoxyethyl)-thiosemicarbazide (32.3 g) is obtained in the form of a white solid.

後処理

  1. concentrationthe mixture is concentrated to dryness at 20° C. under reduced pressure (20 mm Hg; 2.7 kPa)
  2. customThe yellow syrup obtained
  3. customcrystallises
  4. dissolutionThe solid is dissolved in hot methanol (50 cc)
  5. filtrationthe solution is filtered
  6. additiondiluted with diethyl ether (200 cc)
  7. waitAfter about ten hours at 4° C.
  8. filtrationthe mixture is filtered

出典と根拠

ORDレコード
ord-23d3439258c44b2799689bb58598029a
出典データセット
uspto-grants-1981_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04307233

反応ノート

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