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Ethylene Glycol → HCID 20551713、化合物

HRID 1732211
ノート
印刷プレビュー

反応式

HRID 1732211 の反応式
[CH3:1][O:2][CH:3]([O:10][CH3:11])[CH2:4][NH:5][C:6](=[O:9])[CH2:7][Cl:8].C(O)CO.C1(C)C=CC(S(O)(=O)=O)=CC=1>C(OCC)C>[O:10]1[CH2:11][CH2:1][O:2][CH:3]1[CH2:4][NH:5][C:6](=[O:9])[CH2:7][Cl:8]
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 3

HCID 174Ethylene GlycolHCID 6101p-Toluenesulfonic acidHCID 193700222-Chloro-N-(2,2-dimethoxyethyl)acetamide

生成物 1

HCID 20551713HCID 20551713、化合物

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

N-(2,2-Dimethoxyethyl)-2-chloroacetamide (18.1 grams; 0.10 mole) ethylene glycol (6.82 grams; 0.11 mole) and 10 drops of a solution of one gram of p-toluenesulfonic acid in 100 ml of diethyl ether were charged into a glass reaction vessel fitted with a mechanical stirrer, thermometer, distillation heat and condenser. The mixture was stirred and heated to about 95° C. to 100° C. Byproduct methanol was distilled off. When no further methanol was evolved, the mixture was cooled to room temperature, sodium carbonate (2 grams) was added and the slurry was stirred for a period of about 1 hour. The slurry was then filtered and the filtrate fractionally distilled under reduced pressure the desired product N-(1,3-dioxolan-2-ylmethyl)-2-chloroacetamide was obtained as a fraction boiling at 109° C.-110° C. at 0.15 mm Hg which, when cooled, solidified. The solid had a melting point of 61° C.-63° C.

後処理

  1. customfitted with a mechanical stirrer
  2. distillationthermometer, distillation
  3. temperatureheat
  4. temperatureheated to about 95° C. to 100° C
  5. distillationByproduct methanol was distilled off
  6. additionsodium carbonate (2 grams) was added
  7. stirringthe slurry was stirred for a period of about 1 hour
  8. filtrationThe slurry was then filtered
  9. distillationthe filtrate fractionally distilled under reduced pressure the desired product N-(1,3-dioxolan-2-ylmethyl)-2-chloroacetamide
  10. customwas obtained as a fraction boiling at 109° C.-110° C. at 0.15 mm Hg which, when
  11. temperaturecooled

出典と根拠

ORDレコード
ord-bb6d67765e2c47b09b6ac6dd1eb22a2c
出典データセット
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04237056

反応ノート

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