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Sulfuric Acid → 2-Isopropylaminoethanol sulfate

HRID 989466
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HRID 989466 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

HCID 120973772-Isopropylaminoethanol sulfate

시약·촉매·용매 1

HCID 962Water용매3회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-3a76a26683994169b0cc6f2fb2ada68c
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06639109B1

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