反応式
[CH:1](=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH:10]=[CH2:11].Br[C:14](Br)([F:16])[F:15].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O>CN(C)C(=O)C.[Zn]>[F:15][C:14]([F:16])=[CH:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=[CH2:1]参加物
実験手順
Under an argon atmosphere, a stirred mixture of 101.0 grams (0.60 mole) of 10-undecenal and 251.9 grams (1.20 moles) of dibromodifluoromethane was cooled to 0° to -5° C., and a solution of 314.9 grams (1.20 moles) of triphenylphosphine in 1100 ml of N,N-dimethylacetamide was added dropwise during a five to ten minute period. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature where it was stirred for two hours. After this time a small portion from 70.5 grams (1.20 mole) of zinc powder was added to the reaction mixture. The reaction mixture was warmed to approximately 34° C. with an external heat source to initiate further reaction. Upon commencement of the reaction, the reaction mixture temperature rose to 44° C. The remainder of the 70.5 grams of zinc powder was added portionwise during a ten to twenty minute period. Upon completion of addition, the reaction mixture was warmed to 85°-90° C. where it stirred vigorously for two hours. After this time the reaction mixture was cooled to ambient temperature, and 400 ml of water was added. The reaction mixture was stirred for 30 minutes and then was allowed to stand for 18 hours. After this time the reaction mixture was subjected to a steam distillation using pentane as the extraction solvent. The pentane distillate was concentrated under reduced pressure to a residual oil. The residual oil was heated at 94° C. to remove any N,N-dimethylacetamide. The remaining oil was distilled under reduced pressure, yielding 24.3 grams of 1,1-difluoro-1,11-dodecadiene; b.p. 133° C./66 mm. The nmr spectrum was consistent with the proposed structure.
後処理
- temperaturewas cooled to 0° to -5° C.
- additionUpon completion of addition
- temperatureThe reaction mixture was warmed to approximately 34° C. with an external heat source
- customreaction
- customUpon commencement of the reaction
- customrose to 44° C
- additionUpon completion of addition
- temperaturethe reaction mixture was warmed to 85°-90° C. where it
- stirringstirred vigorously for two hours
- temperatureAfter this time the reaction mixture was cooled to ambient temperature
- stirringThe reaction mixture was stirred for 30 minutes
- waitto stand for 18 hours
- distillationAfter this time the reaction mixture was subjected to a steam distillation
- concentrationThe pentane distillate was concentrated under reduced pressure to a residual oil
- temperatureThe residual oil was heated at 94° C.
- customto remove any N,N-dimethylacetamide
- distillationThe remaining oil was distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-f578eee0595e449fabf75d2cd38f5765
- 出典データセット
- uspto-grants-1992_01
- 特許番号
- US05081287
関連ノート
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