Catechol → HCID 131730585, 화합물

HRID 2093270노트

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HRID 2093270 반응식
[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])[OH:2].[O-]CCCC.[Sn+4:14].[O-]CCCC.[O-]CCCC.[O-]CCCC>C1(C)C=CC=CC=1>[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[O-:4])[O-:2].[Sn+4:14].[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[O-:4])[O-:2]

참가 물질

4

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온도
100 °C

실험 절차

A solution of catechol (2.20 g, 20.0 mmol) and toluene (25 ml) was dehydrated by distilling 5 mL of the solution. Thereafter, 4.11 g (10.0 mmol) of tin(IV) butoxide was added to the solution while stirring. The mixed solution was refluxed for 1 hour, and then, while the distillation temperature was 100° C. or higher, distilled until the amount of the solution became half. After the distillation, volatile components of the residual mixed solution were vaporized under reduced pressure by a rotary evaporator. The residual solid content was further heated to 100° C. under vacuum using a vacuum dryer so that the remaining volatile components were completely removed. The solid content (catechol-tin complex) was green in color. The yield amount was 3.35 g (10.0 mmol), and the yield percentage was 100%. 6.70 g of catechol-tin complex was dissolved into 100 mL of 1:4 acetylacetone/toluene to produce a coating liquid.

후처리

  1. distillationby distilling 5 mL of the solution
  2. temperatureThe mixed solution was refluxed for 1 hour
  3. customwas 100° C.
  4. distillationhigher, distilled until the amount of the solution
  5. distillationAfter the distillation, volatile components of the residual mixed solution
  6. customwere vaporized under reduced pressure by a rotary evaporator
  7. customwere completely removed
  8. dissolution6.70 g of catechol-tin complex was dissolved into 100 mL of 1:4 acetylacetone/toluene
  9. customto produce a coating liquid

출처 및 근거

ORD 기록
ord-a3b3024abe8a4a4187a22fa783bc89a2
출처 데이터셋
uspto-grants-2013_05
특허 번호
US08445118B2

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