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Ethyl formate → HCID 178448642, 화합물

HRID 1112105
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HRID 1112105 반응식
[CH2:1]([NH:5][C:6](=[S:9])[NH:7][NH2:8])[CH2:2][CH2:3][CH3:4].C[O-].[Na+].[CH:13](OCC)=O>CO>[SH:9][C:6]1[N:5]([CH2:1][CH2:2][CH2:3][CH3:4])[CH:13]=[N:8][N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8025Ethyl formate2회HCID 18103033-Amino-1-butylthioureaHCID 10942334Sodium Methoxide

생성물 1

HCID 178448642HCID 178448642, 화합물수율 55%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

4-n-Butylthiosemicarbazide (20.0 g. or 0.136 mole) was heated to reflux with a solution of methanol (100 ml.), sodium methoxide (7.55 g. or 0.140 mole) and ethyl formate (20.7 g. or 0.280 mole). After 8 and 16 hours, 10 ml. and 5 ml. of ethyl formate was added to the refluxing solution. After 24 hours total reflux, the solvent was removed under reduced pressure and the residue was dissolved in water (100 ml.). The pH of the solution was adjusted to about 12 with 50% sodium hydroxide solution. This solution was then heated on a steam bath for 45 minutes, cooled and acidified with dilute hydrochloric acid. The resulting oil was extracted into ether. The ether was dried over sodium sulphate and removed under vacuum. The resulting oil was crystallized from ether-hexane to give 11.8 g. (55% yield) of 3-mercapto-4-n-butyl-1,2,4-triazole, m.p. 67°-69° C. The structure was confirmed by its nuclear magnetic resonance spectrum and its mass spectrum.

후처리

  1. customAfter 8 and 16 hours, 10 ml
  2. customthe solvent was removed under reduced pressure
  3. dissolutionthe residue was dissolved in water (100 ml.)
  4. temperatureThis solution was then heated on a steam bath for 45 minutes
  5. temperaturecooled
  6. extractionThe resulting oil was extracted into ether
  7. dry with materialThe ether was dried over sodium sulphate
  8. customremoved under vacuum
  9. customThe resulting oil was crystallized from ether-hexane
  10. customto give 11.8 g

출처 및 근거

ORD 기록
ord-3cfe4e1e47bb41f3ac2bffb27db776f7
출처 데이터셋
uspto-grants-1978_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04120864

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