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Sulfuric Acid → 2-Isopropylaminoethanol sulfate

HRID 989466
ノート
印刷プレビュー

反応式

HRID 989466 の反応式
[S:1](=[O:5])(=[O:4])([OH:3])[OH:2].[CH:6]([NH:9][CH2:10][CH2:11]O)([CH3:8])[CH3:7].C1(C)C=CC=CC=1>O>[S:1]([O:3][CH2:11][CH2:10][NH:9][CH:6]([CH3:8])[CH3:7])([OH:2])(=[O:5])=[O:4]
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 3

HCID 1118Sulfuric AcidHCID 1140TolueneHCID 79942-(Isopropylamino)ethanol

生成物 1

HCID 120973772-Isopropylaminoethanol sulfate

試薬・触媒・溶媒 1

HCID 962Water溶媒3 回

実験手順

In a 50-ml three-necked flask, 1.01 g (10 mmol) of sulfuric acid (97%) was diluted with 1 g of water, and the resulting dilution was ice-cooled. A mixture of 1.03 g (10 mmol) of 2-isopropylaminoethanol and 1 g of water was slowly dropped into the cooled dilution. After completion of the dropping, the resulting mixture was warmed to room temperature and 10 ml of toluene was added thereto. The mixture thus obtained was dehydrated by heating with vigorous stirring after attaching a Dean-Stark trap to the flask. The mixture was heated and stirred for 4 hours until a theoretical amount of water was removed. Then, the reaction was continued for another 1 hour. After a large portion of the toluene was removed by decantation, the residual toluene was distilled off under reduced pressure to obtain a crude product of 2-isopropylaminoethyl hydrogensulfate, the desired compound, quantitatively.

後処理

  1. temperaturecooled
  2. additionwas slowly dropped into the cooled dilution
  3. customThe mixture thus obtained
  4. temperatureby heating
  5. temperatureThe mixture was heated
  6. customwas removed
  7. customAfter a large portion of the toluene was removed by decantation
  8. distillationthe residual toluene was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-3a76a26683994169b0cc6f2fb2ada68c
出典データセット
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06639109B1

反応ノート

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