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Acetic Acid → HCID 14795882, 화합물

HRID 1288631
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HRID 1288631 반응식
[CH2:1]([Sn:5]([CH2:20][CH2:21][CH2:22][CH3:23])([CH2:16][CH2:17][CH2:18][CH3:19])[C:6]1[CH:15]=[CH:14][C:9]([C:10]([O:12]C)=[O:11])=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH3:4].[OH-].[K+].C(O)(=O)C.O>C(O)C>[CH2:20]([Sn:5]([CH2:1][CH2:2][CH2:3][CH3:4])([CH2:16][CH2:17][CH2:18][CH3:19])[C:6]1[CH:15]=[CH:14][C:9]([C:10]([OH:12])=[O:11])=[CH:8][CH:7]=1)[CH2:21][CH2:22][CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 962WaterHCID 14797Potassium HydroxideHCID 13256035Methyl 4-(tributylstannyl)benzoate

생성물 1

HCID 14795882HCID 14795882, 화합물수율 90.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of methyl 4-tri-n-butylstannylbenzoate (3.0 g, 7 mmol) in absolute ethanol (60 ml) was added 0.25 g KOH (9 mmol). The resulting solution was refluxed for 2 hours. The solution was cooled and poured into an ice-cold solution of acetic acid (0.64 g, 10.6 mmol) and water (100 ml). The solution was then extracted with diethyl ether (80 ml). The ether phase was washed with water (30 ml), dried over MgSO4 (5 g), filtered and evaporated under reduced pressure to afford 2.6 g (88%) of the title compound. This material was used without further purification.

후처리

  1. temperatureThe resulting solution was refluxed for 2 hours
  2. temperatureThe solution was cooled
  3. extractionThe solution was then extracted with diethyl ether (80 ml)
  4. washThe ether phase was washed with water (30 ml)
  5. dry with materialdried over MgSO4 (5 g)
  6. filtrationfiltered
  7. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-871560983abd480daa5fe2479ef7f7f5
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05746997

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