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Ethanolamine → 1-Propanesulfonic acid, 3-[(2-hydroxyethyl)amino]-

HRID 437016
ノート
印刷プレビュー

反応式

HRID 437016 の反応式
[CH2:1]([CH2:3][NH2:4])[OH:2].[CH2:5]1[S:9](=[O:11])(=[O:10])[O:8][CH2:7][CH2:6]1>CO>[OH:2][CH2:1][CH2:3][NH:4][CH2:7][CH2:6][CH2:5][S:9]([OH:11])(=[O:10])=[O:8]
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 700EthanolamineHCID 14264Propane sultone

生成物 1

HCID 103134001-Propanesulfonic acid, 3-[(2-hydroxyethyl)amino]-

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

N-(β-hydroxyethyl)-3-aminopropanesulfonic acid, ##STR9## was prepared as follows: 366 parts ethanolamine and 1000 parts methanol were cooled to 10° C. in a three-necked, round-bottom flask which was fitted with a stirring bar, thermometer, and a dropping funnel. 244 parts propane sultone dissolved in 1000 parts methanol were added via the dropping funnel at such a rate that the flask temperature did not increase above 20° C. After the addition was completed, the contents of the flask were stirred for two hours, concentrated to a thick slurry, and then added to 2400 parts isopropyl alcohol. The resulting solid was filtered, rinsed with 500 parts isopropyl alcohol and dried to give 240 parts of the desired product.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customwas fitted with a stirring bar
  2. additionwere added via the dropping funnel at such a rate that the flask temperature
  3. temperaturedid not increase above 20° C
  4. additionAfter the addition
  5. concentrationconcentrated to a thick slurry
  6. additionadded to 2400 parts isopropyl alcohol
  7. filtrationThe resulting solid was filtered
  8. washrinsed with 500 parts isopropyl alcohol
  9. customdried

出典と根拠

ORDレコード
ord-45c146da5c4840a8a650c937bd8e219c
出典データセット
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04029638

反応ノート

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