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Ethanolamine → HCID 22951276、化合物

HRID 276255
ノート
印刷プレビュー

反応式

HRID 276255 の反応式
Br[CH2:2][C:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH:4]=1.[NH2:9][CH2:10][CH2:11][OH:12]>ClC=C(Cl)Cl.[OH-].[Na+]>[OH:12][CH2:11][CH2:10][NH:9][CH2:2][C:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH:4]=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 2

HCID 700EthanolamineHCID 30159321-(Bromomethyl)cyclohexene

生成物 1

HCID 22951276HCID 22951276、化合物収率 62%

試薬・触媒・溶媒 2

HCID 6575Trichloroethylene溶媒HCID 14798Sodium Hydroxide溶媒

実験手順

A solution of 1-bromomethyl-1-cyclohexene (3.25 g) and 2-aminoethanol (6 mL) in trichloroethylene (40 mL) was heated at the reflux temp. for 3 d, cooled to room temp., and diluted with a 1N NaOH solution (30 mL). The aqueous layer was extracted with CH2Cl2 (4×20 mL) and the combined organic layers were washed with H2O (30 mL) and a saturated NaCl solution (30 mL), dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by vacuum distillation to give N-hydroxyethyl-N-cyclohex-1-enylmethylamine as a colorless oil (1.78 g, 62%): bp 92-94° C. (6 mmHg),

後処理

  1. temperaturecooled to room temp.
  2. extractionThe aqueous layer was extracted with CH2Cl2 (4×20 mL)
  3. washthe combined organic layers were washed with H2O (30 mL)
  4. dry with materiala saturated NaCl solution (30 mL), dried (Na2SO4)
  5. concentrationconcentrated under reduced pressure
  6. distillationThe residue was purified by vacuum distillation

出典と根拠

ORDレコード
ord-b364ae2a91544f22b589f234249abcce
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06353006B1

反応ノート

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