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1,1,1-Trimethoxybutane → HCID 20323690、化合物

HRID 839580
ノート
印刷プレビュー

反応式

HRID 839580 の反応式
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[C:6]([NH:8][NH2:9])=[O:7].CO[C:12](OC)(OC)[CH2:13][CH2:14][CH3:15]>C(O)C>[CH2:13]([C:12]1[N:1]2[CH:5]=[CH:4][N:3]=[C:2]2[C:6](=[O:7])[NH:8][N:9]=1)[CH2:14][CH3:15]
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 1235121,1,1-TrimethoxybutaneHCID 12493320HCID 12493320、化合物

生成物 1

HCID 20323690HCID 20323690、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of 37.0 gm. of 2-imidazolecarboxylic acid hydrazide, prepared by the method of U.S. Pat. No. 3,600,399, 2.5 liters of ethanol and 325 ml. of trimethylorthobutyrate is refluxed overnight and evaporated to a solid. This solid is ground, added to 400 ml. of diphenyl ether and heated in an oil bath at 220°-245° C. for 30 minutes. The mixture is cooled to room temperature and crystallized by the addition of 100 ml. of petroleum ether. The solid is collected, washed twice with petroleum ether, recrystallized from 300 ml. of a hot mixture of ethanol and methanol and treated with charcoal giving 53.5 gm. of the desired final product, m.p. 153°-159° C.

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. additionA mixture of 37.0 gm
  2. customevaporated to a solid
  3. additionadded to 400 ml
  4. temperatureof diphenyl ether and heated in an oil bath at 220°-245° C. for 30 minutes
  5. customcrystallized by the addition of 100 ml
  6. customThe solid is collected
  7. washwashed twice with petroleum ether
  8. customrecrystallized from 300 ml
  9. additionof a hot mixture of ethanol and methanol
  10. additiontreated with charcoal giving 53.5 gm

出典と根拠

ORDレコード
ord-f2f3836aa9174430b6c7906139cb523b
出典データセット
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04096257

反応ノート

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