2-Norbornene → Beta-Pinene
反応式
[C:1]12[CH2:9][CH:5]([C:6]1([CH3:8])[CH3:7])[CH2:4][CH2:3][C:2]=2[CH3:10].C12CC(CC1)C=C2.FC1C(B(C2C(F)=C(F)C(F)=C(F)C=2F)C2C(F)=C(F)C(F)=C(F)C=2F)=C(F)C(F)=C(F)C=1F.C([Al](CC)CC)C>C1CCCCC1.C(OC(=O)CCCCC)C.[Ni].[Ni].CO.ClC1C=CC=CC=1>[CH3:7][C:6]1([CH3:8])[CH:1]2[CH2:9][CH:5]1[CH2:4][CH2:3][C:2]2=[CH2:10]参加物
実験手順
To a 50 ml glass vial equipped with a Teflon® coated stirbar was added -pinene (2.5 ml), norbornene (5 g, 53.1 mmol) and chlorobenzene (35 ml). To this stirred solution at ambient temperature was added nickel ethylhexanoate (0.01 ml of an 8% w nickel solution in mineral spirits, 13 μmol) tris(pentafluorophenyl)boron (117 μmol in petroleum naphtha) and triethylaluminum (0.077 ml of a 1.7 molar solution in cyclohexane, 130 μmol). Immediately upon addition of the trialkylaluminum the reaction mixture became yellow and hot. The reaction was allowed to run for 60 minutes after which time methanol (3 ml) was injected to kill the reaction and the resulting solution was poured into excess methanol. The polymer was filtered off and washed with excess methanol and dried overnight in a heated vacuum oven to afford the copolymer (4.0 g). GPC analysis showed the polymer to have a molecular weight (Mw) of 39,800 and a polydispersity of 2.1.
後処理
- customthe reaction
- filtrationThe polymer was filtered off
- washwashed with excess methanol
- customdried overnight in a heated vacuum oven
出典と根拠
- ORDレコード
- ord-88c985e030da47ff82ed69c6c301dd97
- 出典データセット
- uspto-grants-1997_10
- 特許番号
- US05677405
反応ノート
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