Thioxanthone → 9-cyclopropyl-9H-thioxanthen-9-ol

HRID 234668

반응식

HRID 234668 반응식
[CH:1]1([Mg]Br)[CH2:3][CH2:2]1.[CH:6]1[C:19]2[C:18](=[O:20])[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[S:11][C:10]=2[CH:9]=[CH:8][CH:7]=1.[Cl-].[NH4+]>C1COCC1.O>[CH:1]1([C:18]2([OH:20])[C:17]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[S:11][C:10]3[C:19]2=[CH:6][CH:7]=[CH:8][CH:9]=3)[CH2:3][CH2:2]1

참가 물질

6

반응물 3

HCID 10295ThioxanthoneHCID 25517Ammonium ChlorideHCID 178418630HCID 178418630, 화합물

생성물 1

HCID 187993359-cyclopropyl-9H-thioxanthen-9-ol

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of cyclopropylmagnesium bromide in dry THF (prepared from cyclopropylbromide (18.2 g, 0.15 mol), magnesium turnings (2.9 g, 0.12 mol) and dry THF (80 ml)) was placed under an atmosphere of nitrogen. A solution of thioxanthen-9-one (12.7 g, 0.06 mol) in dry THF (70 ml) was added dropwise and when addition was complete the mixture was heated at reflux for 20 minutes. The reaction mixture was cooled on an ice-bath and saturated ammonium chloride (70 ml) was carefully added. The mixture was diluted with water (100 ml) and extracted with diethyl ether (2×100 ml). The combined organic extracts were washed with water, dried (Na2SO4) and the solvent was evaporated in vacuo to give 25.2 g of crude 9-cyclopropyl-9H-thioxanthen-9-ol.

후처리

  1. additionwhen addition
  2. temperaturewas heated
  3. temperatureat reflux for 20 minutes
  4. temperatureThe reaction mixture was cooled on an ice-bath
  5. extractionextracted with diethyl ether (2×100 ml)
  6. washThe combined organic extracts were washed with water
  7. dry with materialdried (Na2SO4)
  8. customthe solvent was evaporated in vacuo

출처 및 근거

ORD 기록
ord-19d9116f4a0740c0be5aae1d7fba87f3
출처 데이터셋
uspto-grants-1997_01
특허 번호
US05595989

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