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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Sulfide → HCID 178478026, 화합물

HRID 363745
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HRID 363745 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5].C([N:12](CC)CC)C.S.[NH2:18][NH2:19].N([O-])=O.[Na+]>CO>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]1[NH:5][N:12]=[N:19][N:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 402Hydrogen SulfideHCID 8471TriethylamineHCID 9321HydrazineHCID 133912-ChlorobenzonitrileHCID 23668193Sodium Nitrite

생성물 1

HCID 178478026HCID 178478026, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

First, 35.6 mmol of 2-chlorobenzonitrile was dissolved in 50 ml of methanol, and 35.6 mmol of triethylarnine and 105 mmol of hydrogen sulfide were added thereto at room temperature, followed by adding 180 mmol of anhydrous hydrazine and keeping at the reflux temperature for 48 hours. The reaction mixture was evaporated under reduced pressure. The residue was dissolved in 50 ml of 5% hydrochloric acid, and 75 mmol of sodium nitrite was added thereto at 0° C. to cause reaction. After completion of the reaction, the reaction mixture was extracted with ethyl acetate to give 5-(2-chlorophenyl)tetrazole. Yield, 54%

후처리

  1. customat room temperature
  2. customThe reaction mixture was evaporated under reduced pressure
  3. dissolutionThe residue was dissolved in 50 ml of 5% hydrochloric acid
  4. customat 0° C.
  5. customreaction
  6. customAfter completion of the reaction
  7. extractionthe reaction mixture was extracted with ethyl acetate

출처 및 근거

ORD 기록
ord-27853476a6b94f57a0de9886991d656d
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05874593

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