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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Acetaldehyde → 2H-1,3-oxazine, tetrahydro-2,4,4,6-tetramethyl-

HRID 848400
ノート
印刷プレビュー

反応式

HRID 848400 の反応式
[CH3:1][C:2]([NH2:8])([CH2:4][CH:5]([OH:7])[CH3:6])[CH3:3].[CH:9](=O)[CH3:10].C1(C)C=CC=CC=1>O>[CH3:9][CH:10]1[NH:8][C:2]([CH3:3])([CH3:1])[CH2:4][CH:5]([CH3:6])[O:7]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

5

反応物 3

HCID 177AcetaldehydeHCID 1140TolueneHCID 954054-Amino-4-methylpentan-2-ol

生成物 1

HCID 118048782H-1,3-oxazine, tetrahydro-2,4,4,6-tetramethyl-収率 94%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
20 °C

実験手順

1,170 parts by weight of 2-methyl-2-aminopentan-4-ol is placed in a stirred flask. With external cooling, 440 parts by weight of acetaldehyde is run in over a period of about 40 minutes at 15°-20° C. The reaction mixture is stirred for a further 15 minutes at 20° C. After the addition of 600 parts by volume of toluene, 182 parts by weight of water is separated off over a period of 2 hours by azeotropic distillation. The reaction product is subjected to fractional distillation. After removal of the solvent there is obtained 1,372 parts by weight of 2,4,4,6-tetramethyltetrahydro-1,3-oxazine with a purity (according to gas chromatography) of 98%, equivalent to a yield of 94% of theory, based on 2-methyl-2-aminopentan-4-ol.

後処理

  1. customis run in over a period of about 40 minutes at 15°-20° C
  2. customis separated off over a period of 2 hours by azeotropic distillation
  3. distillationThe reaction product is subjected to fractional distillation
  4. customAfter removal of the solvent there

出典と根拠

ORDレコード
ord-10ae905908454cffa09763f229166ec0
出典データセット
uspto-grants-1981_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04295875

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