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Trimethyl orthobeznoate → HCID 20323691, 화합물

HRID 839581
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HRID 839581 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)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(O)C>[C:13]1([C:12]2[N:1]3[CH:5]=[CH:4][N:3]=[C:2]3[C:6](=[O:7])[NH:8][N:9]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 69720Trimethyl orthobeznoateHCID 12493320HCID 12493320, 화합물

생성물 1

HCID 20323691HCID 20323691, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A 2.6 gm. portion of 2-imidazolecarboxylic acid hydrazide is added to 200 ml. of ethanol. To this is added 20 ml. of trimethylorthobenzoate. The mixture is refluxed for 31 hours, then the solvents are evaporated giving a white solid which is washed twice with diethyl ether giving 3.0 gm. of white solid. This solid is combined with 50 ml. of diphenyl ether and heated with stirring in an oil bath at 265°-275° C. for 10 minutes. The mixture is cooled, petroleum ether is added and the mixture is filtered. The solid is washed twice with hot petroleum ether, giving 1.4 gm. of the desired product as a light tan solid, m.p. 292°-295° C.

후처리

  1. additionTo this is added 20 ml
  2. temperatureThe mixture is refluxed for 31 hours
  3. customthe solvents are evaporated
  4. customgiving a white solid which
  5. washis washed twice with diethyl ether giving 3.0 gm
  6. temperatureof diphenyl ether and heated
  7. temperatureThe mixture is cooled
  8. additionpetroleum ether is added
  9. filtrationthe mixture is filtered
  10. washThe solid is washed twice with hot petroleum ether
  11. customgiving 1.4 gm

출처 및 근거

ORD 기록
ord-f8ec96467a4c423aad6f340a91e45337
출처 데이터셋
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04096257

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