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Formaldehyde → 3-(1,3-Oxazinan-3-YL)propan-1-OL

HRID 438023
ノート
印刷プレビュー

反応式

HRID 438023 の反応式
[OH:1][CH2:2][CH2:3][CH2:4][NH:5][CH2:6][CH2:7][CH2:8][OH:9].[CH2:10]=O>C1(C)C=CC=CC=1>[OH:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:6][CH2:7][CH2:8][O:9][CH2:10]1
参加物反応条件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 712Formaldehyde2 回HCID 106986Dipropanolamine

生成物 1

HCID 214277223-(1,3-Oxazinan-3-YL)propan-1-OL

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
90 °C

実験手順

To a glass reaction vessel equipped with stirrer, thermometer, and condenser fitted with a water trap is added di-(3-hydroxypropyl) amine (3.0 mole, 399 g.) and toluene (500 g.). Paraformaldehyde (3.15 mole, 90% pure, 105 g.) is weighed out and about 1/3 is added to the amine solution. The resulting mixture is stirred and heated to 90° C. while slowly adding the remaining paraformaldehyde in about 70 minutes. The reaction is heated to reflux and the water separated. After 4 hours, a total of 63 ml. of water is removed. Toluene is removed at reduced pressure. The residue is distilled at high vacuum to yield 3-(γ-hydroxypropyl)tetrahydro-1,3-oxazine.

後処理

  1. customTo a glass reaction vessel
  2. customequipped with stirrer
  3. customthermometer, and condenser fitted with a water trap
  4. temperatureThe reaction is heated
  5. temperatureto reflux
  6. customthe water separated
  7. customof water is removed
  8. customToluene is removed at reduced pressure
  9. distillationThe residue is distilled at high vacuum

出典と根拠

ORDレコード
ord-89c86ce49c384346b9e4ebcb96f0fb50
出典データセット
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04032686

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート