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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Chlorocyclohepta-2,4,6-trien-1-one → 2-Sulfanylcyclohepta-2,4,6-trien-1-one

HRID 2420484
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인쇄 미리보기

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HRID 2420484 반응식
Cl[C:2]1[C:3](=[O:9])[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1.[Na+].[SH-:11]>C(O)C>[SH:11][C:2]1[C:3](=[O:9])[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 196912-Chlorocyclohepta-2,4,6-trien-1-oneHCID 28015Sodium hydrosulfide

생성물 1

HCID 125576902-Sulfanylcyclohepta-2,4,6-trien-1-one

시약·촉매·용매 1

HCID 702Ethanol용매2회

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온도
-70 °C

실험 절차

A solution of 2-chloro-2,4,6-cycloheptatrien-1-one [2.82 g, described by T. Nozoe et al., Proc. Japan Acad., 28, 483 (1952)] in ethanol (20 ml) is added dropwise to a suspension, cooled to -70° C, of sodium sulfhydrate (2.2 g) in ethanol (20 ml). The mixture is stirred at -70° C for two hours, allowed to warm to room temperature and stirred at room temperature for 1 hour. The mixture is filtered and the filtrate is evaporated. The residue is suspended in water, the mixture is acidified to pH2 with 10% hydrochloric acid and extracted with ethyl acetate. The organic extract is dried and evaporated. The residue is dissolved in benzene and subjected to chromatography on silica gel. Th eluates are evaporated to give the title compound, mp 55° C.

후처리

  1. temperatureto warm to room temperature
  2. stirringstirred at room temperature for 1 hour
  3. filtrationThe mixture is filtered
  4. customthe filtrate is evaporated
  5. extractionextracted with ethyl acetate
  6. extractionThe organic extract
  7. customis dried
  8. customevaporated
  9. dissolutionThe residue is dissolved in benzene
  10. customTh eluates are evaporated

출처 및 근거

ORD 기록
ord-42444e5928b147f7ab9c160ddfcc2f5a
출처 데이터셋
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04110468

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