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1,1,1-Trimethoxybutane → HCID 20323690, 화합물

HRID 839580
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HRID 839580 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1235121,1,1-TrimethoxybutaneHCID 12493320HCID 12493320, 화합물

생성물 1

HCID 20323690HCID 20323690, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-f2f3836aa9174430b6c7906139cb523b
출처 데이터셋
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04096257

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